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Sample records for porous polymer coatings

  1. 21 CFR 888.3565 - Knee joint patellofemorotibial metal/polymer porous-coated uncemented prosthesis.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 8 2013-04-01 2013-04-01 false Knee joint patellofemorotibial metal/polymer... Devices § 888.3565 Knee joint patellofemorotibial metal/polymer porous-coated uncemented prosthesis. (a) Identification. A knee joint patellofemorotibial metal/polymer porous-coated uncemented prosthesis is a...

  2. 21 CFR 888.3565 - Knee joint patellofemorotibial metal/polymer porous-coated uncemented prosthesis.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 8 2012-04-01 2012-04-01 false Knee joint patellofemorotibial metal/polymer... Devices § 888.3565 Knee joint patellofemorotibial metal/polymer porous-coated uncemented prosthesis. (a) Identification. A knee joint patellofemorotibial metal/polymer porous-coated uncemented prosthesis is a...

  3. 21 CFR 888.3565 - Knee joint patellofemorotibial metal/polymer porous-coated uncemented prosthesis.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 8 2014-04-01 2014-04-01 false Knee joint patellofemorotibial metal/polymer... Devices § 888.3565 Knee joint patellofemorotibial metal/polymer porous-coated uncemented prosthesis. (a) Identification. A knee joint patellofemorotibial metal/polymer porous-coated uncemented prosthesis is a...

  4. 21 CFR 888.3565 - Knee joint patellofemorotibial metal/polymer porous-coated uncemented prosthesis.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 8 2010-04-01 2010-04-01 false Knee joint patellofemorotibial metal/polymer... Devices § 888.3565 Knee joint patellofemorotibial metal/polymer porous-coated uncemented prosthesis. (a) Identification. A knee joint patellofemorotibial metal/polymer porous-coated uncemented prosthesis is a...

  5. 21 CFR 888.3565 - Knee joint patellofemorotibial metal/polymer porous-coated uncemented prosthesis.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 8 2011-04-01 2011-04-01 false Knee joint patellofemorotibial metal/polymer... Devices § 888.3565 Knee joint patellofemorotibial metal/polymer porous-coated uncemented prosthesis. (a) Identification. A knee joint patellofemorotibial metal/polymer porous-coated uncemented prosthesis is a...

  6. Enhanced photoluminescence of porous silicon nanoparticles coated by bioresorbable polymers

    NASA Astrophysics Data System (ADS)

    Gongalsky, Maxim B.; Kharin, Alexander Yu; Osminkina, Liubov A.; Timoshenko, Victor Yu; Jeong, Jinyoung; Lee, Han; Chung, Bong Hyun

    2012-08-01

    A significant enhancement of the photoluminescence (PL) efficiency is observed for aqueous suspensions of porous silicon nanoparticles (PSiNPs) coated by bioresorbable polymers, i.e., polylactic-co-glycolic acid (PLGA) and polyvinyl alcohol (PVA). PSiNPs with average size about 100 nm prepared by mechanical grinding of electrochemically etched porous silicon were dispersed in water to prepare the stable suspension. The inner hydrophobic PLGA layer prevents the PSiNPs from the dissolution in water, while the outer PVA layer makes the PSiNPs hydrophilic. The PL quantum yield of PLGA/PVA-coated PSiNPs was found to increase by three times for 2 weeks of the storage in water. The observed effect is explained by taking into account both suppression of the dissolution of PSiNPs in water and a process of the passivation of nonradiative defects in PSiNPs. The obtained results are interesting in view of the potential applications of PSiNPs in bioimaging.

  7. Porous palladium coated conducting polymer nanoparticles for ultrasensitive hydrogen sensors.

    PubMed

    Lee, Jun Seop; Kim, Sung Gun; Cho, Sunghun; Jang, Jyongsik

    2015-12-28

    Hydrogen, a clean-burning fuel, is of key importance to various industrial applications, including fuel cells and in the aerospace and automotive industries. However, hydrogen gas is odorless, colorless, and highly flammable; thus appropriate safety protocol implementation and monitoring are essential. Highly sensitive hydrogen leak detection and surveillance sensor systems are needed; additionally, the ability to maintain uniformity through repetitive hydrogen sensing is becoming increasingly important. In this report, we detail the fabrication of porous palladium coated conducting polymer (3-carboxylate polypyrrole) nanoparticles (Pd@CPPys) to detect hydrogen gas. The Pd@CPPys are produced by means of facile alkyl functionalization and chemical reduction of a pristine 3-carboxylate polypyrrole nanoparticle-contained palladium precursor (PdCl(2)) solution. The resulting Pd@CPPy-based sensor electrode exhibits ultrahigh sensitivity (0.1 ppm) and stability toward hydrogen gas at room temperature due to the palladium sensing layer. PMID:26598964

  8. Porous palladium coated conducting polymer nanoparticles for ultrasensitive hydrogen sensors

    NASA Astrophysics Data System (ADS)

    Lee, Jun Seop; Kim, Sung Gun; Cho, Sunghun; Jang, Jyongsik

    2015-12-01

    Hydrogen, a clean-burning fuel, is of key importance to various industrial applications, including fuel cells and in the aerospace and automotive industries. However, hydrogen gas is odorless, colorless, and highly flammable; thus appropriate safety protocol implementation and monitoring are essential. Highly sensitive hydrogen leak detection and surveillance sensor systems are needed; additionally, the ability to maintain uniformity through repetitive hydrogen sensing is becoming increasingly important. In this report, we detail the fabrication of porous palladium coated conducting polymer (3-carboxylate polypyrrole) nanoparticles (Pd@CPPys) to detect hydrogen gas. The Pd@CPPys are produced by means of facile alkyl functionalization and chemical reduction of a pristine 3-carboxylate polypyrrole nanoparticle-contained palladium precursor (PdCl2) solution. The resulting Pd@CPPy-based sensor electrode exhibits ultrahigh sensitivity (0.1 ppm) and stability toward hydrogen gas at room temperature due to the palladium sensing layer.Hydrogen, a clean-burning fuel, is of key importance to various industrial applications, including fuel cells and in the aerospace and automotive industries. However, hydrogen gas is odorless, colorless, and highly flammable; thus appropriate safety protocol implementation and monitoring are essential. Highly sensitive hydrogen leak detection and surveillance sensor systems are needed; additionally, the ability to maintain uniformity through repetitive hydrogen sensing is becoming increasingly important. In this report, we detail the fabrication of porous palladium coated conducting polymer (3-carboxylate polypyrrole) nanoparticles (Pd@CPPys) to detect hydrogen gas. The Pd@CPPys are produced by means of facile alkyl functionalization and chemical reduction of a pristine 3-carboxylate polypyrrole nanoparticle-contained palladium precursor (PdCl2) solution. The resulting Pd@CPPy-based sensor electrode exhibits ultrahigh sensitivity (0.1 ppm

  9. 21 CFR 888.3358 - Hip joint metal/polymer/metal semi-constrained porous-coated uncemented prosthesis.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 8 2010-04-01 2010-04-01 false Hip joint metal/polymer/metal semi-constrained... Devices § 888.3358 Hip joint metal/polymer/metal semi-constrained porous-coated uncemented prosthesis. (a) Identification. A hip joint metal/polymer/metal semi-constrained porous-coated uncemented prosthesis is a...

  10. 21 CFR 888.3535 - Knee joint femorotibial (uni-compartmental) metal/polymer porous-coated uncemented prosthesis.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    .../polymer porous-coated uncemented prosthesis. 888.3535 Section 888.3535 Food and Drugs FOOD AND DRUG... Devices § 888.3535 Knee joint femorotibial (uni-compartmental) metal/polymer porous-coated uncemented prosthesis. (a) Identification. A knee joint femorotibial (uni-compartmental) metal/polymer...

  11. 21 CFR 888.3358 - Hip joint metal/polymer/metal semi-constrained porous-coated uncemented prosthesis.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 8 2011-04-01 2011-04-01 false Hip joint metal/polymer/metal semi-constrained... Devices § 888.3358 Hip joint metal/polymer/metal semi-constrained porous-coated uncemented prosthesis. (a) Identification. A hip joint metal/polymer/metal semi-constrained porous-coated uncemented prosthesis is a...

  12. 21 CFR 888.3535 - Knee joint femorotibial (uni-compartmental) metal/polymer porous-coated uncemented prosthesis.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    .../polymer porous-coated uncemented prosthesis. 888.3535 Section 888.3535 Food and Drugs FOOD AND DRUG... Devices § 888.3535 Knee joint femorotibial (uni-compartmental) metal/polymer porous-coated uncemented prosthesis. (a) Identification. A knee joint femorotibial (uni-compartmental) metal/polymer...

  13. "Thunderstruck": Plasma-Polymer-Coated Porous Silicon Microparticles As a Controlled Drug Delivery System.

    PubMed

    McInnes, Steven J P; Michl, Thomas D; Delalat, Bahman; Al-Bataineh, Sameer A; Coad, Bryan R; Vasilev, Krasimir; Griesser, Hans J; Voelcker, Nicolas H

    2016-02-01

    Controlling the release kinetics from a drug carrier is crucial to maintain a drug's therapeutic window. We report the use of biodegradable porous silicon microparticles (pSi MPs) loaded with the anticancer drug camphothecin, followed by a plasma polymer overcoating using a loudspeaker plasma reactor. Homogenous "Teflon-like" coatings were achieved by tumbling the particles by playing AC/DC's song "Thunderstruck". The overcoating resulted in a markedly slower release of the cytotoxic drug, and this effect correlated positively with the plasma polymer coating times, ranging from 2-fold up to more than 100-fold. Ultimately, upon characterizing and verifying pSi MP production, loading, and coating with analytical methods such as time-of-flight secondary ion mass spectrometry, scanning electron microscopy, thermal gravimetry, water contact angle measurements, and fluorescence microscopy, human neuroblastoma cells were challenged with pSi MPs in an in vitro assay, revealing a significant time delay in cell death onset. PMID:26836366

  14. Hydroxyapatite porous scaffold engineered with biological polymer hybrid coating for antibiotic Vancomycin release.

    PubMed

    Kim, Hae-Won; Knowles, Jonathan C; Kim, Hyoun-Ee

    2005-03-01

    The purpose of this study is to improve hydroxyapatite (HA) porous scaffolds via coating with biological polymer-HA hybrids for use as wound healing and tissue regeneration. Highly porous HA scaffolds, fabricated by a polyurethane foam reticulate method, were coated with hybrid coating solution, consisting of poly(epsilon-caprolactone) (PCL), HA powders, and the antibiotic Vancomycin. The PCL to HA ratio was fixed at 1.5 and the drug amounts were varied [drug/(PCL + HA) = 0.02 and 0.04]. For the purpose of comparison, bare HA scaffold without the hybrid coating layer was also loaded with Vancomycin via an immersion-adsorption method. The hybrid coating structure and morphology were observed with Fourier transformed infrared (FT-IR) spectroscopy and scanning electron microscopy (SEM). The effects of the hybrid coating on the compressive mechanical properties and the in vitro drug release of the scaffolds were investigated in comparison with bare HA scaffold. The PCL-HA hybrid coating altered the scaffold pore structure slightly, resulting in thicker stems and reduced porosity. With the hybrid coating, the HA scaffold responded to an applied compressive stress more effectively without showing a brittle failure. This was attributed to the shielding and covering of the framework surface by the coating layer. The encapsulated drugs within the coated scaffold was released in a highly sustained manner as compared to the rapid release of drugs directly adsorbed on the pure HA scaffold. These findings suggest that the coated HA scaffolds expand their applicability in hard tissue regeneration and wound healing substitutes delivering bioactive molecules. PMID:15744609

  15. 21 CFR 888.3535 - Knee joint femorotibial (uni-compartmental) metal/polymer porous-coated uncemented prosthesis.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 8 2014-04-01 2014-04-01 false Knee joint femorotibial (uni-compartmental) metal... Devices § 888.3535 Knee joint femorotibial (uni-compartmental) metal/polymer porous-coated uncemented prosthesis. (a) Identification. A knee joint femorotibial (uni-compartmental) metal/polymer...

  16. 21 CFR 888.3535 - Knee joint femorotibial (uni-compartmental) metal/polymer porous-coated uncemented prosthesis.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 8 2012-04-01 2012-04-01 false Knee joint femorotibial (uni-compartmental) metal... Devices § 888.3535 Knee joint femorotibial (uni-compartmental) metal/polymer porous-coated uncemented prosthesis. (a) Identification. A knee joint femorotibial (uni-compartmental) metal/polymer...

  17. 21 CFR 888.3535 - Knee joint femorotibial (uni-compartmental) metal/polymer porous-coated uncemented prosthesis.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 8 2013-04-01 2013-04-01 false Knee joint femorotibial (uni-compartmental) metal... Devices § 888.3535 Knee joint femorotibial (uni-compartmental) metal/polymer porous-coated uncemented prosthesis. (a) Identification. A knee joint femorotibial (uni-compartmental) metal/polymer...

  18. 21 CFR 888.3670 - Shoulder joint metal/polymer/metal nonconstrained or semi-constrained porous-coated uncemented...

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 8 2010-04-01 2010-04-01 false Shoulder joint metal/polymer/metal nonconstrained... ORTHOPEDIC DEVICES Prosthetic Devices § 888.3670 Shoulder joint metal/polymer/metal nonconstrained or semi-constrained porous-coated uncemented prosthesis. (a) Identification. A shoulder joint...

  19. 21 CFR 888.3670 - Shoulder joint metal/polymer/metal nonconstrained or semi-constrained porous-coated uncemented...

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 8 2011-04-01 2011-04-01 false Shoulder joint metal/polymer/metal nonconstrained... ORTHOPEDIC DEVICES Prosthetic Devices § 888.3670 Shoulder joint metal/polymer/metal nonconstrained or semi-constrained porous-coated uncemented prosthesis. (a) Identification. A shoulder joint...

  20. The influence of polymer concentrations on the structure and mechanical properties of porous polycaprolactone-coated hydroxyapatite scaffolds

    NASA Astrophysics Data System (ADS)

    Zhao, J.; Duan, K.; Zhang, J. W.; Lu, X.; Weng, J.

    2010-05-01

    Polycaprolactone (PCL)-coated porous hydroxyapatite (HA) composite scaffolds were prepared by combining polymer impregnating method with dip-coating method. Three different PCL solution concentrations were used in dip-coating process to improve the mechanical properties of porous HA scaffolds. The results indicated that as the concentration of PCL solution increases the compressive strength significantly increased from 0.09 MPa to 0.51 MPa while the porosity decreased from 90% to 75% for the composite scaffolds. An interlaced structure was found inside the pore wall for all composite scaffolds due to the penetration of PCL. The porous HA/PCL composite scaffolds dip-coated with 10% PCL exhibited optimal combination of mechanical properties and pore interconnectivity, and may be a potential bone candidate for the tissue engineering applications.

  1. Influence of natural organic matter on transport and retention of polymer coated silver nanoparticles in porous media.

    PubMed

    Yang, Xinyao; Lin, Shihong; Wiesner, Mark R

    2014-01-15

    Interactions between organic matter (OM) and engineered polymer coatings as they affect the retention of polyvinylpyrrolidone (PVP) polymer-coated silver nanoparticles (AgNPs) were studied. Two distinct types of OM-cysteine representing low molecular weight multivalent functional groups, and Suwannee River Humic Acid (HA) representing high molecular weight polymers, were investigated with respect to their effects on particle stability in aggregation and deposition. Aggregation of the PVP coated AgNPs (PVP-AgNPs) was enhanced by cysteine addition at high ionic strengths, which was attributed to cysteine binding to the AgNPs and replacing the otherwise steric stabilizing agent PVP. In contrast the addition of HA did not increase aggregation rates and decreased PVP-AgNP deposition to the silica porous medium, consistent with enhanced electrosteric stabilization by the HA. Although cysteine also reduced deposition in the porous medium, the mechanisms of reduced deposition appear to be enhanced electric double layer (EDL) interaction at low ionic strengths. At higher ionic strengths, aggregation was favored leading to lower deposition due to smaller diffusion coefficients and single collector efficiencies despite the reduced EDL interactions. PMID:24295767

  2. Porous Shape Memory Polymers

    PubMed Central

    Hearon, Keith; Singhal, Pooja; Horn, John; Small, Ward; Olsovsky, Cory; Maitland, Kristen C.; Wilson, Thomas S.; Maitland, Duncan J.

    2013-01-01

    Porous shape memory polymers (SMPs) include foams, scaffolds, meshes, and other polymeric substrates that possess porous three-dimensional macrostructures. Porous SMPs exhibit active structural and volumetric transformations and have driven investigations in fields ranging from biomedical engineering to aerospace engineering to the clothing industry. The present review article examines recent developments in porous SMPs, with focus given to structural and chemical classification, methods of characterization, and applications. We conclude that the current body of literature presents porous SMPs as highly interesting smart materials with potential for industrial use. PMID:23646038

  3. Porous polymer media

    DOEpatents

    Shepodd, Timothy J.

    2002-01-01

    Highly crosslinked monolithic porous polymer materials for chromatographic applications. By using solvent compositions that provide not only for polymerization of acrylate monomers in such a fashion that a porous polymer network is formed prior to phase separation but also for exchanging the polymerization solvent for a running buffer using electroosmotic flow, the need for high pressure purging is eliminated. The polymer materials have been shown to be an effective capillary electrochromatographic separations medium at lower field strengths than conventional polymer media. Further, because of their highly crosslinked nature these polymer materials are structurally stable in a wide range of organic and aqueous solvents and over a pH range of 2-12.

  4. 21 CFR 888.3358 - Hip joint metal/polymer/metal semi-constrained porous-coated uncemented prosthesis.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... titanium-aluminum-vanadium (Ti-6Al-4V) alloy and an acetabular component composed of an ultra-high... titanium or Ti-6Al-4V alloy. The porous coating has a volume porosity between 30 and 70 percent, an...

  5. 21 CFR 888.3358 - Hip joint metal/polymer/metal semi-constrained porous-coated uncemented prosthesis.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... titanium-aluminum-vanadium (Ti-6Al-4V) alloy and an acetabular component composed of an ultra-high... titanium or Ti-6Al-4V alloy. The porous coating has a volume porosity between 30 and 70 percent, an...

  6. 21 CFR 888.3358 - Hip joint metal/polymer/metal semi-constrained porous-coated uncemented prosthesis.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... titanium-aluminum-vanadium (Ti-6Al-4V) alloy and an acetabular component composed of an ultra-high... titanium or Ti-6Al-4V alloy. The porous coating has a volume porosity between 30 and 70 percent, an...

  7. Antibacterial polymer coatings.

    SciTech Connect

    Wilson, Mollye C.; Allen, Ashley N.; Barnhart, Meghan; Tucker, Mark David; Hibbs, Michael R.

    2009-09-01

    A series of poly(sulfone)s with quaternary ammonium groups and another series with aldehyde groups are synthesized and tested for biocidal activity against vegetative bacteria and spores, respectively. The polymers are sprayed onto substrates as coatings which are then exposed to aqueous suspensions of organisms. The coatings are inherently biocidal and do not release any agents into the environment. The coatings adhere well to both glass and CARC-coated coupons and they exhibit significant biotoxicity. The most effective quaternary ammonium polymers kills 99.9% of both gram negative and gram positive bacteria and the best aldehyde coating kills 81% of the spores on its surface.

  8. Optical ammonia gas sensor based on a porous silicon rugate filter coated with polymer-supported dye.

    PubMed

    Shang, Yunling; Wang, Xiaobo; Xu, Erchao; Tong, Changlun; Wu, Jianmin

    2011-01-24

    An ammonia gas sensor chip was prepared by coating an electrochemically-etched porous Si rugate filter with a chitosan film that is crosslinked by glycidoxypropyltrimethoxysilane (GPTMS). The bromothylmol blue (BTB), a pH indicator, was loaded in the film as ammonia-sensing molecules. White light reflected from the porous Si has a narrow bandwidth spectrum with a peak at 610 nm. Monitoring reflective optical intensity at the peak position allows for direct, real-time observation of changes in the concentration of ammonia gas in air samples. The reflective optical intensity decreased linearly with increasing concentrations of ammonia gas over the range of 0-100 ppm. The lowest detection limit was 0.5 ppm for ammonia gas. At optimum conditions, the full response time of the ammonia gas sensor was less than 15s. The sensor chip also exhibited a good long-term stability over 1 year. Therefore, the simple sensor design has potential application in miniaturized optical measurement for online ammonia gas detection. PMID:21168552

  9. Antithrombogenic Polymer Coating.

    DOEpatents

    Huang, Zhi Heng; McDonald, William F.; Wright, Stacy C.; Taylor, Andrew C.

    2003-01-21

    An article having a non-thrombogenic surface and a process for making the article are disclosed. The article is formed by (i) coating a polymeric substrate with a crosslinked chemical combination of a polymer having at least two amino substituted side chains, a crosslinking agent containing at least two crosslinking functional groups which react with amino groups on the polymer, and a linking agent containing a first functional group which reacts with a third functional group of the crosslinking agent, and (ii) contacting the coating on the substrate with an antithrombogenic agent which covalently bonds to a second functional group of the linking agent. In one example embodiment, the polymer is a polyamide having amino substituted alkyl chains on one side of the polyamide backbone, the crosslinking agent is a phosphine having the general formula (A).sub.3 P wherein A is hydroxyalkyl, the linking agent is a polyhydrazide and the antithrombogenic agent is heparin.

  10. Thermal Spray Formation of Polymer Coatings

    NASA Technical Reports Server (NTRS)

    Coquill, Scott; Galbraith, Stephen L.; Tuss. Darren L.; Ivosevic, Milan

    2008-01-01

    This innovation forms a sprayable polymer film using powdered precursor materials and an in-process heating method. This device directly applies a powdered polymer onto a substrate to form an adherent, mechanically-sound, and thickness-regulated film. The process can be used to lay down both fully dense and porous, e.g., foam, coatings. This system is field-deployable and includes power distribution, heater controls, polymer constituent material bins, flow controls, material transportation functions, and a thermal spray apparatus. The only thing required for operation in the field is a power source. Because this method does not require solvents, it does not release the toxic, volatile organic compounds of previous methods. Also, the sprayed polymer material is not degraded because this method does not use hot combustion gas or hot plasma gas. This keeps the polymer from becoming rough, porous, or poorly bonded.

  11. Transport and deposition of polymer-modified Fe0 nanoparticles in 2-D heterogeneous porous media: effects of particle concentration, Fe0 content, and coatings.

    PubMed

    Phenrat, Tanapon; Cihan, Abdullah; Kim, Hye-Jin; Mital, Menka; Illangasekare, Tissa; Lowry, Gregory V

    2010-12-01

    Concentrated suspensions of polymer-modified Fe(0) nanoparticles (NZVI) are injected into heterogeneous porous media for groundwater remediation. This study evaluated the effect of porous media heterogeneity and the dispersion properties including particle concentration, Fe(0) content, and adsorbed polymer mass and layer thickness which are expected to affect the delivery and emplacement of NZVI in heterogeneous porous media in a two-dimensional (2-D) cell. Heterogeneity in hydraulic conductivity had a significant impact on the deposition of NZVI. Polymer modified NZVI followed preferential flow paths and deposited in the regions where fluid shear is insufficient to prevent NZVI agglomeration and deposition. NZVI transported in heterogeneous porous media better at low particle concentration (0.3 g/L) than at high particle concentrations (3 and 6 g/L) due to greater particle agglomeration at high concentration. High Fe(0) content decreased transport during injection due to agglomeration promoted by magnetic attraction. NZVI with a flat adsorbed polymeric layer (thickness ∼30 nm) could not be transported effectively due to pore clogging and deposition near the inlet, while NZVI with a more extended adsorbed layer thickness (i.e., ∼70 nm) were mobile in porous media. This study indicates the importance of characterizing porous media heterogeneity and NZVI dispersion properties as part of the design of a robust delivery strategy for NZVI in the subsurface. PMID:21058703

  12. Stretchable and strong cellulose nanopaper structures based on polymer-coated nanofiber networks: an alternative to nonwoven porous membranes from electrospinning.

    PubMed

    Sehaqui, Houssine; Morimune, Seira; Nishino, Takashi; Berglund, Lars A

    2012-11-12

    Nonwoven membranes based on electrospun fibers are of great interest in applications such as biomedical, filtering, and protective clothing. The poor mechanical performance is a limitation, as is some of the electrospinning solvents. To address these problems, porous nonwoven membranes based on nanofibrillated cellulose (NFC) modified by a hydroxyethyl cellulose (HEC) polymer coating are prepared. NFC/HEC aqueous suspensions are subjected to simple vacuum filtration in a paper-making fashion, followed by supercritical CO(2) drying. These nonwoven nanocomposite membranes are truly nanostructured and exhibit a nanoporous network structure with high specific surface area, as analyzed by nitrogen adsorption and FE-SEM. Mechanical properties evaluated by tensile tests show high strength combined with remarkably high strain to failure of up to 55%. XRD analysis revealed significant fibril realignment during tensile stretching. After postdrawing of the random mats, the modulus and strength are strongly increased. The present preparation route uses components from renewable resources, is environmentally friendly, and results in permeable membranes of exceptional mechanical performance. PMID:23046114

  13. Propagation of polymer slugs through porous media

    SciTech Connect

    Lecourtier, J.; Chauveteau, G.

    1984-09-01

    This paper describes an experimental and theoretical study of the mechanisms governing polymer slug propagation through porous media. An analytical model taking into account the macromolecule exclusion from pore walls is proposed to predict rodlike polymer velocity in porous media and thus the spreading out of polydispersed polymer slugs. Under conditions where this wall exclusion is maximum, i.e. at low shear rates and polymer concentrations, the experiments show that xanthan propagation is effectively predicted by this model. At higher flow rates and polymer concentrations, the effects of hydrodynamic dispersion and viscous fingering are analyzed. A new fractionation method for determining molecular weight distribution of polymers used in EOR is proposed.

  14. Thiazolothiazole-linked porous organic polymers

    DOE PAGESBeta

    Zhu, Xiang; Tian, Chengcheng; Jin, Tian; Wang, Jitong; Mahurin, Shannon Mark; Mei, Wenwen; Xiong, Yan; Hu, Jun; Feng, Xinliang; Liu, Honglai; et al

    2014-10-07

    In this study, thiazolothiazole-linked porous organic polymers have been synthesized from a facile catalyst-free condensation reaction between aldehydes and dithiooxamide under solvothermal conditions. The resultant porous frameworks exhibit a highly selective uptake of CO2 over N2 under ambient conditions.

  15. Thiazolothiazole-linked porous organic polymers

    SciTech Connect

    Zhu, Xiang; Tian, Chengcheng; Jin, Tian; Wang, Jitong; Mahurin, Shannon Mark; Mei, Wenwen; Xiong, Yan; Hu, Jun; Feng, Xinliang; Liu, Honglai; Dai, Sheng

    2014-10-07

    In this study, thiazolothiazole-linked porous organic polymers have been synthesized from a facile catalyst-free condensation reaction between aldehydes and dithiooxamide under solvothermal conditions. The resultant porous frameworks exhibit a highly selective uptake of CO2 over N2 under ambient conditions.

  16. Adsorption Kinetics in Nanoscale Porous Coordination Polymers

    SciTech Connect

    Nune, Satish K.; Thallapally, Praveen K.; McGrail, Benard Peter; Annapureddy, Harsha V. R.; Dang, Liem X.; Mei, Donghai; Karri, Naveen; Alvine, Kyle J.; Olszta, Matthew J.; Arey, Bruce W.; Dohnalkova, Alice

    2015-10-07

    Nanoscale porous coordination polymers were synthesized using simple wet chemical method. The effect of various polymer surfactants on colloidal stability and shape selectivity was investigated. Our results suggest that the nanoparticles exhibited significantly improved adsorption kinetics compared to bulk crystals due to decreased diffusion path lengths and preferred crystal plane interaction.

  17. Oxidation protection coatings for polymers

    NASA Technical Reports Server (NTRS)

    Mirtich, M. J.; Sovey, J. S.; Banks, B. A. (Inventor)

    1985-01-01

    A polymeric substrate is coated with a metal oxide film to provide oxidation protection in low Earth orbital environments. The film contains about 4 volume percent polymer to provide flexibility. A coil of polymer material moves through an ion beam as it is fed between reels. The ion beam first cleans the polymer material surface and then sputters the film material from a target onto this surface.

  18. Microfluidic devices and methods including porous polymer monoliths

    DOEpatents

    Hatch, Anson V; Sommer, Gregory J; Singh, Anup K; Wang, Ying-Chih; Abhyankar, Vinay V

    2014-04-22

    Microfluidic devices and methods including porous polymer monoliths are described. Polymerization techniques may be used to generate porous polymer monoliths having pores defined by a liquid component of a fluid mixture. The fluid mixture may contain iniferters and the resulting porous polymer monolith may include surfaces terminated with iniferter species. Capture molecules may then be grafted to the monolith pores.

  19. Microfluidic devices and methods including porous polymer monoliths

    SciTech Connect

    Hatch, Anson V.; Sommer, Gregory j.; Singh, Anup K.; Wang, Ying-Chih; Abhyankar, Vinay

    2015-12-01

    Microfluidic devices and methods including porous polymer monoliths are described. Polymerization techniques may be used to generate porous polymer monoliths having pores defined by a liquid component of a fluid mixture. The fluid mixture may contain iniferters and the resulting porous polymer monolith may include surfaces terminated with iniferter species. Capture molecules may then be grafted to the monolith pores.

  20. Electrically conductive polymer concrete coatings

    DOEpatents

    Fontana, J.J.; Elling, D.; Reams, W.

    1988-05-26

    A sprayable electrically conductive polymer concrete coating for vertical and overhead applications is described. The coating is permeable yet has low electrical resistivity (<10 ohm-cm), good bond strength to concrete substrates, and good weatherability. A preferred formulation contains about 60 wt% calcined coke breeze, 40 wt% vinyl ester resin with 3.5 wt% modified bentonite clay. Such formulations apply evenly and provide enough rigidity for vertical or overhead structures so there is no drip or sag. 4 tabs.

  1. Electrically conductive polymer concrete coatings

    DOEpatents

    Fontana, J.J.; Elling, D.; Reams, W.

    1990-03-13

    A sprayable electrically conductive polymer concrete coating for vertical d overhead applications is described. The coating is permeable yet has low electrical resistivity (<10 ohm-cm), good bond strength to concrete substrates, and good weatherability. A preferred formulation contains about 60 wt % calcined coke breeze, 40 wt % vinyl ester with 3.5 wt % modified bentonite clay. Such formulations apply evenly and provide enough rigidity for vertical or overhead structures so there is no drip or sag.

  2. Electrically conductive polymer concrete coatings

    DOEpatents

    Fontana, Jack J.; Elling, David; Reams, Walter

    1990-01-01

    A sprayable electrically conductive polymer concrete coating for vertical d overhead applications is described. The coating is permeable yet has low electrical resistivity (<10 ohm-cm), good bond strength to concrete substrates, and good weatherability. A preferred formulation contains about 60 wt % calcined coke breeze, 40 wt % vinyl ester with 3.5 wt % modified bentonite clay. Such formulations apply evenly and provide enough rigidity for vertical or overhead structures so there is no drip or sag.

  3. Thin film-coated polymer webs

    DOEpatents

    Wenz, Robert P.; Weber, Michael F.; Arudi, Ravindra L.

    1992-02-04

    The present invention relates to thin film-coated polymer webs, and more particularly to thin film electronic devices supported upon a polymer web, wherein the polymer web is treated with a purifying amount of electron beam radiation.

  4. A Novel Method to Make Breath Figure Patterns by Spin Coating under Dry Environment: One-step Preparation of Porous Polymer Films

    NASA Astrophysics Data System (ADS)

    Park, Min Soo; Kim, Jin Kon

    2004-03-01

    We introduce a novel method for fabricating breath figure patterns on a homopolymer film by spin coating of polymer solutions with various solvents. The homopolymers employed in this study were cellulose acetate butyrate (CAB), mono-carboxylated end-functional polystyrene (PS-mCOOH) and poly(methyl methacrylate) (PMMA). Breath figure patterns were generated even when a water-miscible solvent such as tetrahydrofuran (THF) was used as a solvent. We even succeeded in generating breath figure patterns by spin coating even under a dry environment (relative humidity less than 30 With the combination of the spin coating method, pores with few hundreds nanometers to several micrometers have been generated. We found that the pore size becomes larger with increasing water content in THF solution and decreasing rotating speed. This is equivalent to increasing humidity and decreasing evaporation speed, respectively, in the conventional method, direct solvent evaporation under a humid environment. Thus, compared with the conventional method for making breath figure patterns, this method would be very convenient for fabricating large-scale films with various pore sizes.

  5. Porous Polyolefin Films via Polymer Blends

    NASA Astrophysics Data System (ADS)

    Macosko, Chris

    Porous polymer films have broad application including battery separators, membrane supports and filters. Polyolefins are attractive for these applications because of their solvent resistance, low electrical and thermal conductivity, easy fabrication and cost. We will describe fabrication of porous films using cocontinuous blends of a polyolefin with another polymer which can be readily removed with a solvent. Methods to image and control the cocontinuous morphology will be presented.Bell, J. R., K. Chang, C. R. Lopez-Barron, C. W. Macosko, and D. C. Morse, ''Annealing of cocontinuous polymer blends: effect of block copolymer molecular weight and architecture,'' Macromolecules 43, 5024-5032 (2010).Lopez-Barron, C. R., and C. W. Macosko, ''Direct measurement of interface anisotropy of bicontinuous structures via 3D image analysis,'' Langmuir 26, 14284-14293 (2010).Trifkovic, M., A. T. Hedegaard, K. Huston, M. Sheikhzadeh, and C. W. Macosko, ''Porous films via PE/PEO cocontinuous blends,'' Macromolecules 45, 6036-6044 (2012).Hedegaard, A.T., L.L. Gu and C. W. Macosko, ``Effect of Extensional Viscosity on Cocontinuity of Immiscible Polymer Blends'' J. Rheol. 59, 1397-1417 (2015).

  6. Distributed Pore Chemistry in Porous Organic Polymers

    NASA Technical Reports Server (NTRS)

    Koontz, Steven L. (Inventor)

    1998-01-01

    A method for making a biocompatible polymer article using a uniform atomic oxygen treatment is disclosed. The sub-strate may be subsequently optionally grated with a compatibilizing compound. Compatibilizing compounds may include proteins, phosphorylcholine groups, platelet adhesion preventing polymers, albumin adhesion promoters, and the like. The compatibilized substrate may also have a living cell layer adhered thereto. The atomic oxygen is preferably produced by a flowing afterglow microwave discharge, wherein the substrate resides in a sidearm out of the plasma. Also, methods for culturing cells for various purposes using the various membranes are disclosed as well. Also disclosed are porous organic polymers having a distributed pore chemistry (DPC) comprising hydrophilic and hydrophobic region, and a method for making the DPC by exposing the polymer to atomic oxygen wherein the rate of hydrophilization is greater than the rate of mass loss.

  7. Distributed Pore Chemistry in Porous Organic Polymers

    NASA Technical Reports Server (NTRS)

    Koontz, Steven L. (Inventor)

    1999-01-01

    A method for making a biocompatible polymer article using a uniform atomic oxygen treatment is disclosed. The substrate may be subsequently optionally grated with a compatibilizing compound. Compatibilizing compounds may include proteins, phosphorylcholine groups, platelet adhesion preventing polymers, albumin adhesion promoters, and the like. The compatibilized substrate may also have a living cell layer adhered thereto. The atomic oxygen is preferably produced by a flowing afterglow microwave discharge. wherein the substrate resides in a sidearm out of the plasma. Also, methods for culturing cells for various purposes using the various membranes are disclosed as well. Also disclosed are porous organic polymers having a distributed pore chemistry (DPC) comprising hydrophilic and hydrophobic regions. and a method for making the DPC by exposing the polymer to atomic oxygen wherein the rate of hydrophilization is greater than the rate of mass loss.

  8. Boron hydride polymer coated substrates

    DOEpatents

    Pearson, Richard K.; Bystroff, Roman I.; Miller, Dale E.

    1987-01-01

    A method is disclosed for coating a substrate with a uniformly smooth layer of a boron hydride polymer. The method comprises providing a reaction chamber which contains the substrate and the boron hydride plasma. A boron hydride feed stock is introduced into the chamber simultaneously with the generation of a plasma discharge within the chamber. A boron hydride plasma of ions, electrons and free radicals which is generated by the plasma discharge interacts to form a uniformly smooth boron hydride polymer which is deposited on the substrate.

  9. Boron hydride polymer coated substrates

    DOEpatents

    Pearson, R.K.; Bystroff, R.I.; Miller, D.E.

    1986-08-27

    A method is disclosed for coating a substrate with a uniformly smooth layer of a boron hydride polymer. The method comprises providing a reaction chamber which contains the substrate and the boron hydride plasma. A boron hydride feed stock is introduced into the chamber simultaneously with the generation of a plasma discharge within the chamber. A boron hydride plasma of ions, electrons and free radicals which is generated by the plasma discharge interacts to form a uniformly smooth boron hydride polymer which is deposited on the substrate.

  10. Production of porous coating on a prosthesis

    DOEpatents

    Sump, Kenneth R.

    1987-01-01

    Preselected surface areas of a prosthesis are covered by a blend of matching primary metallic particles and expendable particles. The particles are compressed and heated to assure that deformation and metallurgical bonding occurs between them and between the primary particles and the surface boundaries of the prosthesis. Porosity is achieved by removal of the expendable material. The result is a coating including discrete bonded particles separated by a network of interconnected voids presenting a homogeneous porous coating about the substrate. It has strength suitable for bone implant usage without intermediate adhesives, and adequate porosity to promote subsequent bone ingrowth.

  11. Nanoparticle/Polymer Nanocomposite Bond Coat or Coating

    NASA Technical Reports Server (NTRS)

    Miller, Sandi G.

    2011-01-01

    This innovation addresses the problem of coatings (meant to reduce gas permeation) applied to polymer matrix composites spalling off in service due to incompatibility with the polymer matrix. A bond coat/coating has been created that uses chemically functionalized nanoparticles (either clay or graphene) to create a barrier film that bonds well to the matrix resin, and provides an outstanding barrier to gas permeation. There is interest in applying clay nanoparticles as a coating/bond coat to a polymer matrix composite. Often, nanoclays are chemically functionalized with an organic compound intended to facilitate dispersion of the clay in a matrix. That organic modifier generally degrades at the processing temperature of many high-temperature polymers, rendering the clay useless as a nano-additive to high-temperature polymers. However, this innovation includes the use of organic compounds compatible with hightemperature polymer matrix, and is suitable for nanoclay functionalization, the preparation of that clay into a coating/bondcoat for high-temperature polymers, the use of the clay as a coating for composites that do not have a hightemperature requirement, and a comparable approach to the preparation of graphene coatings/bond coats for polymer matrix composites.

  12. Inorganic nanoparticles in porous coordination polymers.

    PubMed

    Kim, Cho Rong; Uemura, Takashi; Kitagawa, Susumu

    2016-07-21

    Porous coordination polymers (PCPs) have been recently highlighted because of their high synthetic designability in structure and functions. Because of their ordered nanoporous structures with a large surface area and tunable pore surface functionality, PCPs have emerged as a significant class of nanoporous materials with potential applications in gas storage, separation, catalysis, and chemical sensing. Recent research has shown the utility of PCPs as host materials for the confinement of nanoparticles of inorganic polymers (IPs), such as metals, metal oxides, and metal chalcogenides. The fabrication of IP nanoparticles in PCPs (PCP⊃IP) has been studied for manifesting specific nanosized-dependent properties and host-guest synergistic functions. In this review, we describe the recent progress in the accommodation of IPs in the nanochannels of PCPs and the remarkable functions of the composite materials. PMID:27051891

  13. Polymer-Coated Graphene Aerogel Beads and Supercapacitor Application.

    PubMed

    Ouyang, An; Cao, Anyuan; Hu, Song; Li, Yanhui; Xu, Ruiqiao; Wei, Jinquan; Zhu, Hongwei; Wu, Dehai

    2016-05-01

    Graphene aerogels are highly porous materials with many energy and environmental applications; tailoring the structure and composition of pore walls within the aerogel is the key to those applications. Here, by freeze casting the graphene oxide sheets, we directly fabricated freestanding porous graphene beads containing radially oriented through channels from the sphere center to its surface. Furthermore, we introduced pseudopolymer to make reinforced, functional composite beads with a unique pore morphology. We showed that polymer layers can be coated smoothly on both sides of the pore walls, as well as on the junctions between adjacent pores, resulting in uniform polymer-graphene-polymer sandwiched structures (skeletons) throughout the bead. These composite beads significantly improved the electrochemical properties, with specific capacitances up to 669 F/g and good cyclic stability. Our results indicate that controlled fabrication of homogeneous hierarchical structures is a potential route toward high performance composite electrodes for various energy applications. PMID:27058391

  14. Spray forming polymer membranes, coatings and films

    DOEpatents

    McHugh, K.M.; Watson, L.D.; McAtee, R.E.; Ploger, S.A.

    1993-10-12

    A method is described for forming a polymer film having controlled physical and chemical characteristics, wherein a plume of nebulized droplets of a polymer or polymer precursor is directed toward a substrate from a converging/diverging nozzle having a throat at which the polymer or a precursor thereof is introduced and an exit from which the nebulized droplets of the polymer or precursor thereof leave entrained in a carrier gas. Relative movement between the nozzle and the substrate is provided to form a polymer film. Physical and chemical characteristics can be controlled by varying the deposition parameters and the gas and liquid chemistries. Semipermeable membranes of polyphosphazene films are disclosed, as are a variety of other polymer systems, both porous and non-porous. 4 figures.

  15. Spray forming polymer membranes, coatings and films

    DOEpatents

    McHugh, Kevin M.; Watson, Lloyd D.; McAtee, Richard E.; Ploger, Scott A.

    1993-01-01

    A method of forming a polymer film having controlled physical and chemical characteristics, wherein a plume of nebulized droplets of a polymer or polymer precursor is directed toward a substrate from a converging/diverging nozzle having a throat at which the polymer or a precursor thereof is introduced and an exit from which the nebulized droplets of the polymer or precursor thereof leave entrained in a carrier gas. Relative movement between the nozzle and the substrate is provided to form a polymer film. Physical and chemical characteristics can be controlled by varying the deposition parameters and the gas and liquid chemistries. Semipermeable membranes of polyphosphazene films are disclosed, as are a variety of other polymer systems, both porous and non-porous.

  16. Electrocatalysts using porous polymers and method of preparation

    DOEpatents

    Liu, Di-Jia; Yuan, Shengwen; Goenaga, Gabriel A.

    2016-08-02

    A method of producing an electrocatalyst article using porous polymers. The method creates a porous polymer designed to receive transition metal groups disposed at ligation sites and activating the transition metals to form an electrocatalyst which can be used in a fuel cell. Electrocatalysts prepared by this method are also provided. A fuel cell which includes the electrocatalyst is also provided.

  17. Organosiloxane-grafted natural polymer coatings

    DOEpatents

    Sugama, Toshifumi

    1998-01-01

    A new family of polysaccharide graft polymers are provided as corrosion resistant coatings having antimicrobial properties which are useful on light metals such as aluminum, magnesium, zinc, steel and their alloys. Methods of making the polysaccharide graft polymers are also included. The methods of making the polysaccharide graft polymers involve reacting a polysaccharide source with an antimicrobial agent under conditions of hydrolysis-condensation.

  18. Hierarchical porous polymer scaffolds from block copolymers.

    PubMed

    Sai, Hiroaki; Tan, Kwan Wee; Hur, Kahyun; Asenath-Smith, Emily; Hovden, Robert; Jiang, Yi; Riccio, Mark; Muller, David A; Elser, Veit; Estroff, Lara A; Gruner, Sol M; Wiesner, Ulrich

    2013-08-01

    Hierarchical porous polymer materials are of increasing importance because of their potential application in catalysis, separation technology, or bioengineering. Examples for their synthesis exist, but there is a need for a facile yet versatile conceptual approach to such hierarchical scaffolds and quantitative characterization of their nonperiodic pore systems. Here, we introduce a synthesis method combining well-established concepts of macroscale spinodal decomposition and nanoscale block copolymer self-assembly with porosity formation on both length scales via rinsing with protic solvents. We used scanning electron microscopy, small-angle x-ray scattering, transmission electron tomography, and nanoscale x-ray computed tomography for quantitative pore-structure characterization. The method was demonstrated for AB- and ABC-type block copolymers, and resulting materials were used as scaffolds for calcite crystal growth. PMID:23908232

  19. Porous alumina based ordered nanocomposite coating for wear resistance

    NASA Astrophysics Data System (ADS)

    Yadav, Arti; Muthukumar, M.; Bobji, M. S.

    2016-08-01

    Uniformly dispersed nanocomposite coating of aligned metallic nanowires in a matrix of amorphous alumina is fabricated by pulsed electrodeposition of copper into the pores of porous anodic alumina. Uniform deposition is obtained by controlling the geometry of the dendritic structure at the bottom of pores through stepwise voltage reduction followed by mild etching. The tribological behaviour of this nanocomposite coating is evaluated using a ball on flat reciprocating tribometer under the dry contact conditions. The nanocomposite coating has higher wear resistance compared to corresponding porous alumina coating. Wear resistant nanocomposite coating has wide applications especially in protecting the internal surfaces of aluminium internal combustion engines.

  20. Osteogenecity of octacalcium phosphate coatings applied on porous metal implants.

    PubMed

    Barrère, Florence; van der Valk, Chantal M; Dalmeijer, Remco A J; Meijer, Gert; van Blitterswijk, Clemens A; de Groot, Klaas; Layrolle, Pierre

    2003-09-15

    The biomimetic route allows the homogeneous deposition of calcium phosphate (Ca-P) coatings on porous implants by immersion in simulated physiologic solution. In addition, various Ca-P phases, such as octacalcium phosphate (OCP) or bone-like carbonated apatite (BCA), which are stable only at low temperatures, can be deposited. In this pilot study, experiments were designed with a twofold-purpose: (1) to investigate the osteoinduction of OCP-coated and noncoated porous tantalum cylinders and of dense titanium alloy cylinders (5 mm in diameter and 10 mm in length) in the back muscle of goats at 12 and 24 weeks (n = 4); and (2) to compare the osteogenic potentials of BCA-coated, OCP-coated, and bare porous tantalum cylinders in a gap of 1 mm created in the femoral condyle of a goat at 12 weeks (n = 2). In the goat muscle, after 12 weeks the OCP-coated porous cylinder had induced ectopic bone as well as bone within the cavity of the OCP-coated dense titanium cylinder. In the femoral condyle, bone did not fill the gap in any of the porous implants. In contrast with the two other groups, OCP-coated porous cylinders exhibited bone formation in the center of the implant. The nature of the Ca-P coating, via its microstructure, its dissolution rate, and its specific interactions with body fluids, may influence the osteogenecity of the Ca-P biomaterial. PMID:12926029

  1. Antireflective Coatings for Glass and Transparent Polymers.

    PubMed

    Buskens, Pascal; Burghoorn, Marieke; Mourad, Maurice Christian Danho; Vroon, Zeger

    2016-07-12

    Antireflective coatings (ARCs) are applied to reduce surface reflections. We review coatings that reduce the reflection of the surface of the transparent substrates float glass, polyethylene terephthalate, poly(methyl methacrylate), and polycarbonate. Three main coating concepts exist to lower the reflection at the interface of a transparent substrate and air: multilayer interference coatings, graded index coatings, and quarter-wave coatings. We introduce and discuss these three concepts, and zoom in on porous quarter-wave coatings comprising colloidal particles. We extensively discuss the four routes for introducing porosity in quarter-wave coatings through the use of colloidal particles, which have the highest potential for application: (1) packing of dense nanospheres, (2) integration of voids through hollow nanospheres, (3) integration of voids through sacrificial particle templates, and (4) packing of nonspherical nanoparticles. Finally, we address the remaining challenges in the field of ARCs, and elaborate on potential strategies for future research in this area. PMID:27187719

  2. The flow around circular cylinders partially coated with porous media

    NASA Astrophysics Data System (ADS)

    Ruck, Bodo; Klausmann, Katharina; Wacker, Tobias

    2012-05-01

    There are indications that the flow resistance of bodies can be reduced by a porous coating or porous sheath. A few numerical investigations exists in this field, however, experimental evidence is lacking. In order to investigate this phenomenon, the drag resistance of cylinders with porous coating has been investigated qualitatively and quantitatively in wind tunnel experiments. The Reynolds number was systematically varied in the range from 104 to 1.3*105. The results show that the boundary layer over the porous surface is turbulent right from the beginning and thickens faster because of the possible vertical momentum exchange at the interface. The region of flow detachment is widened resulting in a broader area with almost vanishing low flow velocities. All in all, the measurements show that a full porous coating of the cylinders increase the flow resistance. However, the measurements show that a partial coating only on the leeward side can decrease the flow resistance of the body. This effect seems due to the fact that the recirculating velocity and the underpressure in the wake is reduced significantly through a leeward porous coating. Thus, combining a smooth non-permeable windward side with a porous-coated leeward side can lead to a reduction of the body's flow resistance. These findings can be applied advantageously in many technical areas, such as energy saving of moving bodies (cars/trains/planes) or in reducing fluid loads on submersed bodies.

  3. Photoinitiated grafting of porous polymer monoliths and thermoplastic polymers for microfluidic devices

    DOEpatents

    Frechet, Jean M. J.; Svec, Frantisek; Rohr, Thomas

    2008-10-07

    A microfluidic device preferably made of a thermoplastic polymer that includes a channel or a multiplicity of channels whose surfaces are modified by photografting. The device further includes a porous polymer monolith prepared via UV initiated polymerization within the channel, and functionalization of the pore surface of the monolith using photografting. Processes for making such surface modifications of thermoplastic polymers and porous polymer monoliths are set forth.

  4. Preparation of Porous Hydroxyapatite Tablets and Porous Hydroxyapatite Coatings for Orthopaedic Use

    NASA Astrophysics Data System (ADS)

    Méndez-González, M.

    2004-09-01

    Porous hydroxyapatite tablets and coatings on metal substrates were obtained by the addition of polymeric additives and liofilization. Both tablets and coatings were characterized by scanning electron microscopy and x-ray diffraction. Coatings obtained by plasma spraying also exhibited interconnected porous of 100 μm while coatings obtained by laser ablation did not show any porosity. The diffraction patterns of the deposited HA were similar to that of the powder obtained by the precipitation method suggesting that no significant changes occurred during the coating procedure.

  5. Interfacial Characterization of Rigid Polymer Coatings

    NASA Astrophysics Data System (ADS)

    DeNolf, Garret C.

    In order to enhance the performance and durability of today's polymer coatings it is pivotal to be able to characterize their mechanical and chemical properties, with emphasized importance on coating-substrate interfaces which are common points of material failure. The purpose of this thesis was to develop and demonstrate novel characterization methods to measure the interfacial and bulk properties of these polymer films and improve the overall understanding of these materials. The first portion of this thesis explores a new peel test technique to measure the adhesion between substrates and coatings. The employed method examines the effect of processing conditions and substrate treatment on the adhesion of polyurethane coatings. This technique successfully quantifies the adhesion of polyurethane coatings to a variety of treated substrates and at multiple curing temperatures. The second thrust of this thesis involves the utilization of a quartz crystal microbalance instrument to characterize the bulk rheological properties of polymer films and coatings in situ. This novel method enables the examination of the effect of temperature and mixing stoichiometry on the rheological properties of curing polyurethane coatings and polymer films. This analysis is extended to measure the curing and aging of paint systems relevant to the art conservation scientific community. The final portion of this thesis focuses on understanding the effect of pH on the interfacial swelling of polymer films in aqueous environments. The quartz crystal microbalance is used to characterize the swelling of interfacial polymer films as water reaches the interface, and the corresponding permeability and osmotic pressure provides insight into the mechanisms of delamination and adhesive failure of coatings attached to metal surfaces. The novel methods and calculations established in this thesis enable precise measurements of coating interfaces and rheological properties and have considerable potential

  6. Aqueous vinylidene fluoride polymer coating composition

    NASA Technical Reports Server (NTRS)

    Bartoszek, Edward J. (Inventor); Christofas, Alkis (Inventor)

    1978-01-01

    A water-based coating composition which may be air dried to form durable, fire resistant coatings includes dispersed vinylidene fluoride polymer particles, emulsified liquid epoxy resin and a dissolved emulsifying agent for said epoxy resin which agent is also capable of rapidly curing the epoxy resin upon removal of the water from the composition.

  7. Organosiloxane-grafted natural polymer coatings

    DOEpatents

    Sugama, Toshifumi

    1998-12-01

    A new family of polysaccharide graft polymers are provided as corrosion resistant coatings having antimicrobial properties which are useful on light metals such as aluminum, magnesium, zinc, steel and their alloys. Methods of making the polysaccharide graft polymers are also included. The methods of making the polysaccharide graft polymers involve reacting a polysaccharide source with an antimicrobial agent under conditions of hydrolysis-condensation. 17 figs.

  8. Nanoscale Reinforced, Polymer Derived Ceramic Matrix Coatings

    SciTech Connect

    Rajendra Bordia

    2009-07-31

    The goal of this project was to explore and develop a novel class of nanoscale reinforced ceramic coatings for high temperature (600-1000 C) corrosion protection of metallic components in a coal-fired environment. It was focused on developing coatings that are easy to process and low cost. The approach was to use high-yield preceramic polymers loaded with nano-size fillers. The complex interplay of the particles in the polymer, their role in controlling shrinkage and phase evolution during thermal treatment, resulting densification and microstructural evolution, mechanical properties and effectiveness as corrosion protection coatings were investigated. Fe-and Ni-based alloys currently used in coal-fired environments do not possess the requisite corrosion and oxidation resistance for next generation of advanced power systems. One example of this is the power plants that use ultra supercritical steam as the working fluid. The increase in thermal efficiency of the plant and decrease in pollutant emissions are only possible by changing the properties of steam from supercritical to ultra supercritical. However, the conditions, 650 C and 34.5 MPa, are too severe and result in higher rate of corrosion due to higher metal temperatures. Coating the metallic components with ceramics that are resistant to corrosion, oxidation and erosion, is an economical and immediate solution to this problem. Good high temperature corrosion protection ceramic coatings for metallic structures must have a set of properties that are difficult to achieve using established processing techniques. The required properties include ease of coating complex shapes, low processing temperatures, thermal expansion match with metallic structures and good mechanical and chemical properties. Nanoscale reinforced composite coatings in which the matrix is derived from preceramic polymers have the potential to meet these requirements. The research was focused on developing suitable material systems and

  9. Coated Porous Si for High Performance On-Chip Supercapacitors

    NASA Astrophysics Data System (ADS)

    Grigoras, K.; Keskinen, J.; Grönberg, L.; Ahopelto, J.; Prunnila, M.

    2014-11-01

    High performance porous Si based supercapacitor electrodes are demonstrated. High power density and stability is provided by ultra-thin TiN coating of the porous Si matrix. The TiN layer is deposited by atomic layer deposition (ALD), which provides sufficient conformality to reach the bottom of the high aspect ratio pores. Our porous Si supercapacitor devices exhibit almost ideal double layer capacitor characteristic with electrode volumetric capacitance of 7.3 F/cm3. Several orders of magnitude increase in power and energy density is obtained comparing to uncoated porous silicon electrodes. Good stability of devices is confirmed performing several thousands of charge/discharge cycles.

  10. Coating to enhance metal-polymer adhesion

    SciTech Connect

    Parthasarathi, A.; Mahulikar, D.

    1996-12-31

    An ultra-thin electroplated coating has been developed to enhance adhesion of metals to polymers. The coating was developed for microelectronic packaging applications where it greatly improves adhesion of metal leadframes to plastic molding compounds. Recent tests show that the coating enhances adhesion of different metals to other types of adhesives as well and may thus have wider applicability. Results of adhesion tests with this coating, as well as its other characteristics such as corrosion resistance, are discussed. The coating is a very thin transparent electroplated coating containing zinc and chromium. It has been found to be effective on a variety of metal surfaces including copper alloys, Fe-Ni alloys, Al alloys, stainless steel, silver, nickel, Pd/Ni and Ni-Sn. Contact resistance measurements show that the coating has little or no effect on electrical resistivity.

  11. Surface studies of coated polymer microspheres and protein release from tissue-engineered scaffolds.

    PubMed

    Meese, Thomas M; Hu, Yunhua; Nowak, Richard W; Marra, Kacey G

    2002-01-01

    The controlled release of growth factors from porous, polymer scaffolds is being studied for potential use as tissue-engineered scaffolds. Biodegradable polymer microspheres were coated with a biocompatible polymer membrane to permit the incorporation of the microspheres into tissue-engineered scaffolds. Surface studies with poly(D,L-lactic-co-glycolic acid) [PLGA], and poly(vinyl alcohol) [PVA] were conducted. Polymer films were dip-coated onto glass slides and water contact angles were measured. The contact angles revealed an initially hydrophobic PLGA film, which became hydrophilic after PVA coating. After immersion in water, the PVA coating was removed and a hydrophobic PLGA film remained. Following optimization using these 2D contact angle studies, biodegradable PLGA microspheres were prepared, characterized, and coated with PVA. X-ray photoelectron spectroscopy was used to further characterize coated slides and microspheres. The release of the model protein bovine serum albumin from PVA-coated PLGA microspheres was studied over 8 days. The release of BSA from PVA-coated PLGA microspheres embedded in porous PLGA scaffolds over 24 days was also examined. Coating of the PLGA microspheres with PVA permitted their incorporation into tissue-engineered scaffolds and resulted in a controlled release of BSA. PMID:12022746

  12. Conducting polymers as corrosion resistant coatings

    SciTech Connect

    Wrobleski, D.A.; Benicewicz, B.C.

    1994-09-01

    Although the majority of top coatings used for corrosion protection are electrically insulating, previous workers have proposed using an electrically active barrier for corrosion control. The most effective corrosion resistant undercoatings in use today are based on chromium compounds. Coatings based on other materials will need to replace these coatings by the turn of the century because of environmental and health concerns. For this reason the authors have begun an investigation of the use of conducting polymers as corrosion resistant coatings as an alternative to metal-based coatings. Conducting polymers have long been considered to be unsuitable for commercial processing, hindering their use for practical applications. Research in the field of electrically conducting polymers has recently produced a number of polymers such as polyaniline and its derivatives which are readily soluble in common organic solvents. The authors coating system, consisting of a conducting polyaniline primer layer, topcoated with epoxy or polyurethane, has been evaluated for corrosion resistance on mild steel substrates. In this paper, the authors report the results of laboratory testing under acidic and saline conditions and the results of testing in the severe launch environment at the Beach Testing Facility at Kennedy Space Center. The launch environment consists of exposure to corrosive HCl exhaust fumes and the salt spray from the Atlantic Ocean.

  13. Biocorrosion behavior and cell viability of adhesive polymer coated magnesium based alloys for medical implants

    NASA Astrophysics Data System (ADS)

    Abdal-hay, Abdalla; Dewidar, Montasser; Lim, Jae Kyoo

    2012-11-01

    The present study was ultimately aimed to design novel adhesive biodegradable polymer, poly(vinyl acetate) (PVAc), coatings onto Mg based alloys by the dip-coating technique in order to control the degradation rate and enhance the biocompatibility of magnesium alloys. The influence of various solvents on PVAc surface topography and their protection of Mg alloys were dramatically studied in vitro. Electrochemical polarization, degradation, and PVAc film cytocompatibility were also tested. Our results showed that the solvent had a significant effect on coating quality. PVAc/dichloromethane solution showed a porous structure and solution concentration could control the porous size. The coatings prepared using tetrahydrofuran and dimethylformamide solvents are exceptional in their ability to generate porous morphology even at low polymer concentration. In general, the corrosion performance appears to be different on different PVAc-solvent system. Immersion tests illustrated that the porous morphology on PVAc stabilized corrosion rates. A uniform corrosion attack in artificial simulation body fluid was also exhibited. The cytocompatibility of osteoblast cells (MC3T3) revealed high adherence, proliferation, and survival on the porous structure of PVAc coated Mg alloy, which was not observed for the uncoated samples. This novel PVAc coating is a promising candidate for biodegradable implant materials, which might widen the use of Mg based implants.

  14. Advanced Porous Coating for Low-Density Ceramic Insulation Materials

    NASA Technical Reports Server (NTRS)

    Leiser, Daniel B.; Churchward, Rex; Katvala, Victor; Stewart, David; Balter, Aliza

    1988-01-01

    The need for improved coatings on low-density reusable surface insulation (RSI) materials used on the space shuttle has stimulated research into developing tougher coatings. The processing of a new porous composite "coating" for RST called toughened unipiece fibrous insulation Is discussed. Characteristics including performance in a simulated high-speed atmospheric entry, morphological structure before and after this exposure, resistance to Impact, and thermal response to a typical heat pulse are described. It is shown that this coating has improved impact resistance while maintaining optical and thermal properties comparable to the previously available reaction-cured glass coating.

  15. Macromolecular coatings on porous silicon: Applications in drug delivery, biosensing, and composites

    NASA Astrophysics Data System (ADS)

    Perelman, Loren Avery

    Two classes of macromolecules, proteins and polymers, are coated onto porous Si films in a variety of geometries in order to study fundamental behaviors of these coatings and their potential device applications. The unique preparation control that porous Si allows in both nano-morphology and surface functionalization provides the means for the coatings. In chapter two, a drug delivery platform using bovine serum albumin (BSA) protein as a stimuli-responsive capping layer on porous Si is described and characterized. It was found that the surface chemistry of the porous Si film has a profound influence on both drug loading capacity and drug release kinetics, providing for control over these drug release variables. The BSA is observed to act as a pH-responsive trigger for the release of vancomycin from the porous Si film. The drug is safely stored in the porous matrix at pH 4 and is released after triggering with pH 7.4 phosphate buffered saline. Chapter three discusses a porous SiO2-based biosensor that is prepared by oxidizing a porous Si film, adsorbing BSA to the surface as a coating, and functionalizing the protein with specific target probes for vancomycin. The BSA was observed to adsorb strongly to the surface, resisting desoprtion in both phosphate buffered saline and triton-X buffer solutions. Quantitative binding information for the tripeptide Ac-L-Lysine-D-Alanine-D-Alanine and vancomycin is determined using the optical properties of the porous Si as a transduction methodology. Chapters four and five describe the fabrication of thermoresponsive and multifunctional nanohybrids, respectively, using stimuli-responsive hydrogels to infiltrate and coat oxidized porous Si films. The optical properties of the porous Si films are used to study the response of the hydrogel phase of the hybrids to a variety of stimuli. The optical changes correspond to previously-described physical changes in the hydrogel phase, and it was determined that this platform provides a

  16. Preceramic Polymers for Use as Fiber Coatings

    NASA Technical Reports Server (NTRS)

    Heimann, P. J.; Hurwitz, F. I.; Wheeler, D.; Eldridge, J.; Baranwal, R.; Dickerson, R.

    1996-01-01

    Polymeric precursors to Si-C-O, SI-B-N and Si-C were evaluated for use as ceramic interfaces in ceramic matrix composites. Use of the preceramic polymers allows for easy dip coating of fibers from dilute solutions of a polymer, which are then pyrolyzed to obtain the ceramic. SCS-0 fibers (Textron Specialty Materials, Lowell, MA) were coated with polymers from three systems: polysilsesquioxanes, polyborosilazanes and polycarbosilanes. The polysilsesquioxane systems were shown to produce either silicon oxycarbide or silicon oxynitride, depending on the pyrolysis conditions, and demonstrated some promise in an RBSN (reaction-bonded silicon nitride) matrix model system. Polyborosilazanes were shown, in studies of bulk polymers, to give rise to oxidation resistant Si-B-N ceramics which remain amorphous to temperatures of 1600 C, and should therefore provide a low modulus interface. Polycarbosilanes produce amorphous carbon-rich Si-C materials which have demonstrated oxidation resistance.

  17. Porous carbon-coated graphite electrodes for energy production from salinity gradient using reverse electrodialysis

    NASA Astrophysics Data System (ADS)

    Lee, Su-Yoon; Jeong, Ye-Jin; Chae, So-Ryong; Yeon, Kyeong-Ho; Lee, Yunkyu; Kim, Chan-Soo; Jeong, Nam-Jo; Park, Jin-Soo

    2016-04-01

    Performance of graphite foil electrodes coated by porous carbon black (i.e., Vulcan) was investigated in comparison with metal electrodes for reverse electrodialysis (RED) application. The electrode slurry that was used for fabrication of the porous carbon-coated graphite foil is composed of 7.2 wt% of carbon black (Vulcan X-72), 0.8 wt% of a polymer binder (polyvinylidene fluoride, PVdF), and 92.0 wt% of a mixing solvent (dimethylacetamide, DMAc). Cyclic voltammograms of both the porous carbon (i.e., Vulcan)-coated graphite foil electrode and the graphite foil electrode without Vulcan showed good reversibility in the hexacyanoferrate(III) (i.e., Fe(CN)63-) and hexacyanoferrate(II) (i.e., Fe(CN)64-) redox couple and 1 M Na2SO4 at room temperature. However, anodic and cathodic current of the Vulcan-coated graphite foil electrode was much higher than those of the graphite foil electrode. Using a bench-scale RED stack, the current-voltage polarization curve of the Vulcan-coated graphite electrode was compared to that of metal electrodes such as iridium (Ir) and platinum (Pt). From the results, it was confirmed that resistance of four different electrodes increased with the following order: the Vulcan-coated graphite foilcoated titanium (Ti) meshcoated Ti platecoated graphite foil showed 5-10% higher power density than the metal mesh electrodes. From the polarization curve of the Vulcan-coated graphite foil electrode, it was found that total resistance decreased as thickness and geometric surface area of the electrode increased.

  18. Compressibility of porous TiO2 nanoparticle coating on paperboard

    PubMed Central

    2013-01-01

    Compressibility of liquid flame spray-deposited porous TiO2 nanoparticle coating was studied on paperboard samples using a traditional calendering technique in which the paperboard is compressed between a metal and polymer roll. Surface superhydrophobicity is lost due to a smoothening effect when the number of successive calendering cycles is increased. Field emission scanning electron microscope surface and cross‒sectional images support the atomic force microscope roughness analysis that shows a significant compressibility of the deposited TiO2 nanoparticle coating with decrease in the surface roughness and nanoscale porosity under external pressure. PACS 61.46.-w; 68.08.Bc; 81.07.-b PMID:24160373

  19. Porous silicon photonic crystals as hosts for polymers, biopolymers, and magnetic nanoparticles

    NASA Astrophysics Data System (ADS)

    Li, Yang Yang

    This thesis describes the construction of one-dimensional photonic crystals of porous silicon by electrochemically etching and the use of these materials as hosts for polymers, biopolymers, and magnetic nanoparticles. The spectral features of the photonic crystals derive from a porosity gradient that is determined by the electrochemical etching parameters. Since the photonic crystals are constructed of a porous material, they can serve as hosts for other materials. The first chapter of the thesis provides an introduction to porous Si, templating techniques and the use of porous materials for controlled release of drugs. This latter section is added because much of the thesis work addresses the application of porous Si hosts for controlled release of drugs. In the second chapter, it is shown that the spectral properties of the porous Si photonic crystal template can be transferred to a variety of organic and biopolymers. It is demonstrated that these castings can be used as vapor sensors and as self-reporting, bioresorbable materials. If the template is not removed, porous Si polymer composites are formed. The third chapter discussed that by spray-coating a fine mist of polymer solution onto the porous Si film, robust and smooth micron-sized cylindrical photonic crystals suitable for bioassays can be prepared. The fourth chapter focuses on using porous Si photonic crystals as a host for magnetic nanoparticles. The magnetic nanoparticles in this work are found to adhere to the surface of the porous Si film as well to infiltrate the pore structure. In a demonstration of optical switching that may be useful for information display applications, flipping between the colored to dark sides by application of a magnetic field is found to occur at rates of as large as 175 Hz. As the host for soluble molecular species, porous Si photonic crystals can be impregnated from solution. The aggregates that form upon evaporation of solvent are found to scatter light from the resonant

  20. Electrochemical Impedance Spectroscopy of Conductive Polymer Coatings

    NASA Technical Reports Server (NTRS)

    Calle, Luz Marina; MacDowell, Louis G.

    1996-01-01

    Electrochemical impedance spectroscopy (EIS) was used to investigate the corrosion protection performance of twenty nine proprietary conductive polymer coatings for cold rolled steel under immersion in 3.55 percent NaCl. Corrosion potential as well as Bode plots of the data were obtained for each coating after one hour immersion, All coatings, with the exception of one, have a corrosion potential that is higher in the positive direction than the corrosion potential of bare steel under the same conditions. Group A consisted of twenty one coatings with Bode plots indicative of the capacitive behavior characteristic of barrier coatings. An equivalent circuit consisting of a capacitor in series with a resistor simulated the experimental EIS data for these coatings very well. Group B consisted of eight coatings that exhibited EIS spectra showing an inflection point which indicates that two time constants are present. This may be caused by an electrochemical process taking place which could be indicitive of coating failing. These coatings have a lower impedance that those in Group A.

  1. Porous polymer networks and ion-exchange media and metal-polymer composites made therefrom

    DOEpatents

    Kanatzidis, Mercouri G; Katsoulidis, Alexandros

    2015-03-10

    Porous polymeric networks and composite materials comprising metal nanoparticles distributed in the polymeric networks are provided. Also provided are methods for using the polymeric networks and the composite materials in liquid- and vapor-phase waste remediation applications. The porous polymeric networks, are highly porous, three-dimensional structures characterized by high surface areas. The polymeric networks comprise polymers polymerized from aldehydes and phenolic molecules.

  2. Thermal Imaging Processes of Polymer Nanocomposite Coatings

    NASA Astrophysics Data System (ADS)

    Meth, Jeffrey

    2015-03-01

    Laser induced thermal imaging (LITI) is a process whereby infrared radiation impinging on a coating on a donor film transfers that coating to a receiving film to produce a pattern. This talk describes how LITI patterning can print color filters for liquid crystal displays, and details the physical processes that are responsible for transferring the nanocomposite coating in a coherent manner that does not degrade its optical properties. Unique features of this process involve heating rates of 107 K/s, and cooling rates of 104 K/s, which implies that not all of the relaxation modes of the polymer are accessed during the imaging process. On the microsecond time scale, the polymer flow is forced by devolatilization of solvents, followed by deformation akin to the constrained blister test, and then fracture caused by differential thermal expansion. The unique combination of disparate physical processes demonstrates the gamut of physics that contribute to advanced material processing in an industrial setting.

  3. Transport in Porous Media of Poly(Acrylic Acid) Coated Ferrihydrite Nanoparticles

    NASA Astrophysics Data System (ADS)

    Jaffe, P. R.; Xiang, A.; Koel, B. E.

    2012-12-01

    Augmentation of soils with iron to enhance biological processes such as uranium reduction via iron reducing bacteria, e.g., Geobacter sp., might be achieved via the injection of iron nanoparticles into the subsurface. The challenge is to make these nanoparticles transportable in the subsurface while not affecting the iron bioavailability. Poorly crystallized 2-line ferrihydrite iron oxide nanoparticles were synthesized and coated with different amounts of poly(acrylic acid) polymers (Na-PAA6K or Na-PAA140K). Analyses were then performed on these particles, including sorption/desorption of the polymer onto the iron nanoparticles, particle size, zeta potential, transport in sand and soil columns, and bioavailabity of the Fe(III) in the absence and presence of the coating to iron reducing organisms. Results showed that at pH values of environmental relevance, the zeta potential of the particles varied from about 3 mV (pH=8.2) for the non-coated particles to about -30 mV for the particles coated with the polymers to their highest sorption capacity. The coated particle diameter was shown to be in the range of 200 nm. Column transport experiments showed that for the highest polymer coating the nanoparticle breakthrough was virtually identical to that of bromide, while significant filtration was observed for particles with an intermediate coating, and complete particle removal via filtration was observed for the non-coated particles. These results held for sand as well as for soil, which had been previously characterized, from a field site at Rifle, CO. Bioavailability experiments showed no difference in the iron reduction rate between the untreated and treated nanoparticles. These results show that it is possible to manufacture iron nanoparticles to enhance biological iron reduction, and that the transport properties of these treated particles is tunable so that a desired retention in the porous medium can be achieved.

  4. Plasma-Sprayed Coatings on Porous Surfaces

    NASA Technical Reports Server (NTRS)

    Leibert, C. H.

    1986-01-01

    Need for combining benefits of duplex thermal-barrier coatings with film cooling on gas-turbine vanes and blades stimulated development of improved method for plasma spraying these coatings. Method reduces blocking of holes by plasma-sprayed material and at same time reduces base-metal oxidation during coating operation. Features provide potential for increased engine efficiency and power, reduced fuel consumption, use of less costly materials or construction procedures, and extended life and durability.

  5. Entropy-induced separation of star polymers in porous media

    NASA Astrophysics Data System (ADS)

    Blavats'Ka, V.; von Ferber, C.; Holovatch, Yu.

    2006-09-01

    We present a quantitative picture of the separation of star polymers in a solution where part of the volume is influenced by a porous medium. To this end, we study the impact of long-range-correlated quenched disorder on the entropy and scaling properties of f -arm star polymers in a good solvent. We assume that the disorder is correlated on the polymer length scale with a power-law decay of the pair correlation function g(r)˜r-a . Applying the field-theoretical renormalization group approach we show in a double expansion in ɛ=4-d and δ=4-a that there is a range of correlation strengths δ for which the disorder changes the scaling behavior of star polymers. In a second approach we calculate for fixed space dimension d=3 and different values of the correlation parameter a the corresponding scaling exponents γf that govern entropic effects. We find that γf-1 , the deviation of γf from its mean field value is amplified by the disorder once we increase δ beyond a threshold. The consequences for a solution of diluted chain and star polymers of equal molecular weight inside a porous medium are that star polymers exert a higher osmotic pressure than chain polymers and in general higher branched star polymers are expelled more strongly from the correlated porous medium. Surprisingly, polymer chains will prefer a stronger correlated medium to a less or uncorrelated medium of the same density while the opposite is the case for star polymers.

  6. Entropy-induced separation of star polymers in porous media

    SciTech Connect

    Blavats'ka, V.; Ferber, C. von; Holovatch, Yu.

    2006-09-15

    We present a quantitative picture of the separation of star polymers in a solution where part of the volume is influenced by a porous medium. To this end, we study the impact of long-range-correlated quenched disorder on the entropy and scaling properties of f-arm star polymers in a good solvent. We assume that the disorder is correlated on the polymer length scale with a power-law decay of the pair correlation function g(r){approx}r{sup -a}. Applying the field-theoretical renormalization group approach we show in a double expansion in {epsilon}=4-d and {delta}=4-a that there is a range of correlation strengths {delta} for which the disorder changes the scaling behavior of star polymers. In a second approach we calculate for fixed space dimension d=3 and different values of the correlation parameter a the corresponding scaling exponents {gamma}{sub f} that govern entropic effects. We find that {gamma}{sub f}-1, the deviation of {gamma}{sub f} from its mean field value is amplified by the disorder once we increase {delta} beyond a threshold. The consequences for a solution of diluted chain and star polymers of equal molecular weight inside a porous medium are that star polymers exert a higher osmotic pressure than chain polymers and in general higher branched star polymers are expelled more strongly from the correlated porous medium. Surprisingly, polymer chains will prefer a stronger correlated medium to a less or uncorrelated medium of the same density while the opposite is the case for star polymers.

  7. Porous coatings from wire mesh for bone implants

    DOEpatents

    Sump, Kenneth R.

    1986-01-01

    A method of coating areas of bone implant elements and the resulting implant having a porous coating are described. Preselected surface areas are covered by a preform made from continuous woven lengths of wire. The preform is compressed and heated to assure that diffusion bonding occurs between the wire surfaces and between the surface boundaries of the implant element and the wire surfaces in contact with it. Porosity is achieved by control of the resulting voids between the bonded wire portions.

  8. Microfluidic approach to the formation of internally porous polymer particles by solvent extraction.

    PubMed

    Watanabe, Takaichi; G Lopez, Carlos; Douglas, Jack F; Ono, Tsutomu; Cabral, João T

    2014-03-11

    We report the controlled formation of internally porous polyelectrolyte particles with diameters ranging from tens to hundreds of micrometers through selective solvent extraction using microfluidics. Solvent-resistant microdevices, fabricated by frontal photopolymerization, encapsulate binary polymer (P)/solvent (S1) mixtures by a carrier solvent phase (C) to form plugs with well-defined radii and low polydispersity; the suspension is then brought into contact with a selective extraction solvent (S2) that is miscible with C and S1 but not P, leading to the extraction of S1 from the droplets. The ensuing phase inversion yields polymer capsules with a smooth surface but highly porous internal structure. Depending on the liquid extraction time scale, this stage can be carried out in situ, within the chip, or ex situ, in an external S2 bath. Bimodal polymer plugs are achieved using asymmetrically inverted T junctions. For this demonstration, we form sodium poly(styrenesulfonate) (P) particles using water (S1), hexadecane (C), and methyl ethyl ketone (S2). We measure droplet extraction rates as a function of drop size and polymer concentration and propose a simple scaling model to guide particle formation. We find that the extraction time required to form particles from liquid droplets does not depend on the initial polymer concentration but is rather proportional to the initial droplet size. The resulting particle size follows a linear relationship with the initial droplet size for all polymer concentrations, allowing for the precise control of particle size. The internal particle porous structure exhibits a polymer density gradient ranging from a dense surface skin toward an essentially hollow core. Average particle porosities between 10 and 50% are achieved by varying the initial droplet compositions up to 15 wt % polymer. Such particles have potential applications in functional, optical, and coating materials. PMID:24568261

  9. Moisture sensor based on evanescent wave light scattering by porous sol-gel silica coating

    DOEpatents

    Tao, Shiquan; Singh, Jagdish P.; Winstead, Christopher B.

    2006-05-02

    An optical fiber moisture sensor that can be used to sense moisture present in gas phase in a wide range of concentrations is provided, as well techniques for making the same. The present invention includes a method that utilizes the light scattering phenomenon which occurs in a porous sol-gel silica by coating an optical fiber core with such silica. Thus, a porous sol-gel silica polymer coated on an optical fiber core forms the transducer of an optical fiber moisture sensor according to an embodiment. The resulting optical fiber sensor of the present invention can be used in various applications, including to sense moisture content in indoor/outdoor air, soil, concrete, and low/high temperature gas streams.

  10. Temperature dependence of porous silica antireflective (AR) coating

    NASA Astrophysics Data System (ADS)

    Tang, Yongxing; Le, Yueqin; Zhang, Weiqing; Jiang, Minhua; Sun, Jinren; Liu, Xiaolin

    1998-02-01

    In this paper, the antireflective coatings consisting of porous silica particles from a silica sol are applied by dip method. The relationships among composition, viscosity and temperature have been studied. The coating homogeneity is opium for the laser wavelengths of 1064 nm, 532 nm and 355 nm. The peak transmission of coated BK-7 glass substrate is higher than 99.5%. The laser induced damage thresholds of the antireflective coatings were range of 7 - 10 J/cm2, for 1 ns pulse width and 1064 nm wavelength. These damage thresholds were suitable for our national ICF program. It is noted that the optical homogeneity of coating and the viscosity of coating sol were strongly influenced by the temperatures in the duration of sol ripening.

  11. Electrospun Fibro-porous Polyurethane Coatings for Implantable Glucose Biosensors

    PubMed Central

    Wang, Ning; Burugapalli, Krishna; Song, Wenhui; Halls, Justin; Moussy, Francis; Ray, Asim; Zheng, Yudong

    2012-01-01

    This study reports methods for coating miniature implantable glucose biosensors with electrospun polyurethane (PU) membranes, their effects on sensor function and efficacy as mass-transport limiting membranes. For electrospinning fibres directly on sensor surface, both static and dynamic collector systems, were designed and tested. Optimum collector configurations were first ascertained by FEA modelling. Both static and dynamic collectors allowed complete covering of sensors, but it was the dynamic collector that produced uniform fibro-porous PU coatings around miniature ellipsoid biosensors. The coatings had random fibre orientation and their uniform thickness increased linearly with increasing electrospinning time. The effects of coatings having an even spread of submicron fibre diameters and sub-100μm thicknesses on glucose biosensor function were investigated. Increasing thickness and fibre diameters caused a statistically insignificant decrease in sensor sensitivity for the tested electrospun coatings. The sensors’ linearity for the glucose detection range of 2 to 30mM remained unaffected. The electrospun coatings also functioned as mass-transport limiting membranes by significantly increasing the linearity, replacing traditional epoxy-PU outer coating. To conclude, electrospun coatings, having controllable fibro-porous structure and thicknesses, on miniature ellipsoid glucose biosensors were demonstrated to have minimal effect on pre-implantation sensitivity and also to have mass-transport limiting ability. PMID:23146433

  12. Electrospun fibro-porous polyurethane coatings for implantable glucose biosensors.

    PubMed

    Wang, Ning; Burugapalli, Krishna; Song, Wenhui; Halls, Justin; Moussy, Francis; Ray, Asim; Zheng, Yudong

    2013-01-01

    This study reports methods for coating miniature implantable glucose biosensors with electrospun polyurethane (PU) membranes, their effects on sensor function and efficacy as mass-transport limiting membranes. For electrospinning fibres directly on sensor surface, both static and dynamic collector systems, were designed and tested. Optimum collector configurations were first ascertained by FEA modelling. Both static and dynamic collectors allowed complete covering of sensors, but it was the dynamic collector that produced uniform fibro-porous PU coatings around miniature ellipsoid biosensors. The coatings had random fibre orientation and their uniform thickness increased linearly with increasing electrospinning time. The effects of coatings having an even spread of submicron fibre diameters and sub-100 μm thicknesses on glucose biosensor function were investigated. Increasing thickness and fibre diameters caused a statistically insignificant decrease in sensor sensitivity for the tested electrospun coatings. The sensors' linearity for the glucose detection range of 2-30 mM remained unaffected. The electrospun coatings also functioned as mass-transport limiting membranes by significantly increasing the linearity, replacing traditional epoxy-PU outer coating. To conclude, electrospun coatings, having controllable fibro-porous structure and thicknesses, on miniature ellipsoid glucose biosensors were demonstrated to have minimal effect on pre-implantation sensitivity and also to have mass-transport limiting ability. PMID:23146433

  13. Transparent Aluminium Oxide Coatings of Polymer Brushes.

    PubMed

    Micciulla, Samantha; Duan, XiaoFei; Strebe, Julia; Löhmann, Oliver; Lamb, Robert N; von Klitzing, Regine

    2016-04-11

    A novel method for the preparation of transparent Al2 O3 coatings of polymers is presented. An environmental-friendly sol-gel method is employed, which implies mild conditions and low costs. A thermoresponsive brush is chosen as a model surface. X-ray photoelectron spectroscopy is used to characterize the samples during the conversion of the precursor Al(OH)3 into oxide and to prove the mildness of the protocol. The study evidences a relation between lateral homogeneity of alumina and the wettability of the polymer surface by the precursor solution, while morphology and elasticity are dominated by the polymer properties. The study of the swelling behavior of the underneath brush reveals the absence of water uptake, proving the impermeability of the alumina layer. The broad chemical and structural variety of polymers, combined with the robustness of transparent alumina films, makes these composites promising as biomedical implants, protective sheets and components for electric and optical devices. PMID:26991543

  14. Method for dialysis on microchips using thin porous polymer membrane

    DOEpatents

    Singh, Anup K.; Kirby, Brian J.; Shepodd, Timothy J.

    2009-05-19

    Laser-induced phase-separation polymerization of a porous acrylate polymer is used for in-situ fabrication of dialysis membranes inside glass microchannels. A shaped 355 nm laser beam is used to produce a porous polymer membrane with a thickness of about 15 .mu.m, which bonds to the glass microchannel and forms a semi-permeable membrane. Differential permeation through a membrane formed with pentaerythritol triacrylate was observed and quantified by comparing the response of the membrane to fluorescein and fluorescently tagging 200 nm latex microspheres. Differential permeation was observed and quantified by comparing the response to rhodamine 560 and lactalbumin protein in a membrane formed with SPE-methylene bisacrylamide. The porous membranes illustrate the capability for the present technique to integrate sample cleanup into chip-based analysis systems.

  15. Dialysis on microchips using thin porous polymer membranes

    DOEpatents

    Singh, Anup K.; Kirby, Brian J.; Shepodd, Timothy J.

    2007-09-04

    Laser-induced phase-separation polymerization of a porous acrylate polymer is used for in-situ fabrication of dialysis membranes inside glass microchannels. A shaped 355 nm laser beam is used to produce a porous polymer membrane with a thickness of about 15 .mu.m, which bonds to the glass microchannel and form a semi-permeable membrane. Differential permeation through a membrane formed with pentaerythritol triacrylate was observed and quantified by comparing the response of the membrane to fluorescein and fluorescently tagging 200 nm latex microspheres. Differential permeation was observed and quantified by comparing the response to rhodamine 560 and lactalbumin protein in a membrane formed with SPE-methylene bisacrylamide. The porous membranes illustrate the capability for the present technique to integrate sample cleanup into chip-based analysis systems.

  16. Mechanical properties of crosslinked polymer coatings

    NASA Technical Reports Server (NTRS)

    Csernica, Jeffrey

    1994-01-01

    The objectives of this experiment are to: fabricate and test thin films to explore relations between a polymer's structure and its mechanical properties; expose students to testing methods for hardness and impact energy that are simple to perform and which have results that are easy to comprehend; show importance of polymer properties in materials that students frequently encounter; illustrate a system which displays a tradeoff between strength and impact resistance, the combination of which would need to be optimized for a particular application; and to expose students to coatings technology and testing.

  17. Polymer Coatings Reduce Electro-osmosis

    NASA Technical Reports Server (NTRS)

    Herren, Blair J.; Snyder, Robert; Shafer, Steven G.; Harris, J. Milton; Van Alstine, James M.

    1989-01-01

    Poly(ethylene glycol) film controls electrostatic potential. Electro-osmosis in quartz or glass chambers reduced or reversed by coating inside surface of chambers with monomacromolecular layers of poly(ethylene glycol). Stable over long times. Electrostatic potential across surface of untreated glass or plastic chamber used in electro-phoresis is negative and attracts cations in aqueous electrolyte. Cations solvated, entrains flow of electrolyte migrating toward cathode. Electro-osmotic flow interferes with desired electrophoresis of particles suspended in electrolyte. Polymer coats nontoxic, transparent, and neutral, advantageous for use in electrophoresis.

  18. Thermal Spraying of Bioactive Polymer Coatings for Orthopaedic Applications

    NASA Astrophysics Data System (ADS)

    Chebbi, A.; Stokes, J.

    2012-06-01

    Flame sprayed biocompatible polymer coatings, made of biodegradable and non-biodegradable polymers, were investigated as single coatings on titanium and as top coatings on plasma sprayed Hydroxyapatite. Biocompatible polymers can act as drug carriers for localized drug release following implantation. The polymer matrix consisted of a biodegradable polymer, polyhydroxybutyrate 98%/ polyhydroxyvalerate 2% (PHBV) and a non-biodegradable polymer, polymethylmethacrylate (PMMA). Screening tests were performed to determine the suitable range of spraying parameters, followed by a Design of Experiments study to determine the effects of spraying parameters on coating characteristics (thickness, roughness, adhesion, wettability), and to optimize the coating properties accordingly. Coatings characterization showed that optimized flame sprayed biocompatible polymers underwent little chemical degradation, did not produce acidic by-products in vitro, and that cells proliferated well on their surface.

  19. Unsteady-State Flow of Flexible Polymers in Porous Media.

    PubMed

    Zitha, Pacelli L. J.; Chauveteau, Guy; Léger, Liliane

    2001-02-15

    In this paper we report an investigation of the unsteady-state flow of polymer solutions through granular porous media. The experiments were performed using high-molecular-weight nonionic and anionic polyacrylamides dissolved in water containing NaCl and model porous media obtained by packing silicon carbide (SiC) grains having a narrow grain size distribution. Before injection in porous media, the polymer solutions were carefully filtered according to a method that was proved to be efficient in removing any possibly remaining microgels. The SiC grain surface was passively oxidized by a controlled thermal treatment in order to obtain a surface partially covered by a thin silica layer having adsorption properties similar to those of quartzitic sand. By packing SiC grains of different sizes, porous media having identical adsorption properties and well-known pore throats sizes can be obtained with a good reproducibility. Parameters investigated include pore size, velocity gradient, polymer concentration, and adsorption energy. A striking unsteady-state flow behavior (pressure build-up at constant flow rate) is observed when three conditions are fulfilled: (a) the velocity gradient is larger than that known to be able to induce a coil-stretch transition, (b) the polymer adsorbs on the pore surfaces, and (c) the length of stretched macromolecules is larger than the effective pore throat diameter. When one of these conditions is not satisfied the flow remains steady. These observations are interpreted by a mechanism involving the adsorption and bridging across pore restrictions of elongated chains. We propose to refer to this peculiar mode of polymer adsorption as bridging adsorption. Copyright 2001 Academic Press. PMID:11161513

  20. Physical-chemical and biological characterization of silk fibroin-coated porous membranes for medical applications.

    PubMed

    Cassinelli, C; Cascardo, G; Morra, M; Draghi, L; Motta, A; Catapano, G

    2006-09-01

    Membranes in artificial organs and scaffolds for tissue engineering are often coated with biomimetic molecules (e.g., collagen) to improve their biocompatibility and promote primary cell adhesion and differentiation. However, animal proteins are expensive and may be contaminated with prions. Silk fibroin (SF) made by Bombyx Mori silk worms, used as a scaffold or grafted to other polymers, reportedly promotes the adhesion and growth of many human cell types. This paper describes how commercial porous membranes were physically coated with SF, and their physical-chemical properties were characterized by SEM, AFM, tensile stress analysis and dynamic contact angle measurements. The effect of the SF coating on membrane biocompatibility and resistance to bacterial colonization is also examined. The proposed technique yields SF coats of different thickness that strengthen the membranes and make their surface remarkably more wettable. The SF coat is not cytotoxic, and promotes the adhesion and proliferation of an immortalized fibroblast cell line. Similarly to collagen, SF-coated membranes also exhibit a much better resistance to the adhesion of S. epidermidis bacteria than uncoated membranes. These preliminary results suggest that SF is a feasible alternative to collagen as a biomimetic coating for 3D scaffolds for tissue engineering or bioartificial (as well as artificial) prosthesis. PMID:17033996

  1. Cell-Culture Reactor Having a Porous Organic Polymer Membrane

    NASA Technical Reports Server (NTRS)

    Koontz, Steven L. (Inventor)

    2000-01-01

    A method for making a biocompatible polymer article using a uniform atomic oxygen treatment is disclosed. The substrate may be subsequently optionally grated with a compatibilizing compound. Compatibilizing compounds may include proteins, phosphory1choline groups, platelet adhesion preventing polymers, albumin adhesion promoters, and the like. The compatibilized substrate may also have a living cell layer adhered thereto. The atomic oxygen is preferably produced by a flowing afterglow microwave discharge, wherein the substrate resides in a sidearm out of the plasma. Also, methods for culturing cells for various purposes using the various membranes are disclosed as well. Also disclosed are porous organic polymers having a distributed pore chemistry (DPC) comprising hydrophilic and hydrophobic regions, and a method for making the DPC by exposing the polymer to atomic oxygen wherein the rate of hydrophilization is greater than the rate of mass loss.

  2. Static properties of polymer chains in porous media

    NASA Astrophysics Data System (ADS)

    Honeycutt, J. D.; Thirumalai, D.

    1989-04-01

    The static properties of a polymer molecule in a porous medium are investigated. The porous medium is simulated using a site percolation model in which the various sites are occupied (or unoccupied) randomly. A freely jointed chain is allowed to move in continuous space between the obstacles. Effects of excluded volume interactions between the links have also been studied. Using a generalized Flory theory, we have shown that, when the strength of disorder is large enough, the mean square end-to-end distance scales as N2ν, where N is the number of links in the chain, and ν takes on a value different from that for a free chain. Under these conditions, the polymer assumes a compact, globule-like conformation. For sufficiently large N, the Flory theory gives ν=1/(d+2) for freely jointed chains and ν=1/d for chains with excluded volume. Various correlation functions such as the distribution of the end-to-end distance and density profile of monomers with respect to the center of mass of the chain have been computed using Monte Carlo simulations. These results are interpreted using scaling concepts and an approximate variational theory based on replica methods. The limitations of the replica variational theory are assessed by an application to the directed polymer in a quenched random environment. We have also studied the shape fluctuations that the polymer molecule undergoes in the random environment. It is argued that these shape fluctuations are relevant to the transport mechanism of polymers in random media. The results obtained for the porous media are contrasted with those found for polymers in media where the obstacles are arranged in a regular manner.

  3. Durable polymer-aerogel based superhydrophobic coatings, a composite material

    DOEpatents

    Kissel, David J; Brinker, Charles Jeffrey

    2014-03-04

    Provided are polymer-aerogel composite coatings, devices and articles including polymer-aerogel composite coatings, and methods for preparing the polymer-aerogel composite. The exemplary article can include a surface, wherein the surface includes at least one region and a polymer-aerogel composite coating disposed over the at least one region, wherein the polymer-aerogel composite coating has a water contact angle of at least about 140.degree. and a contact angle hysteresis of less than about 1.degree.. The polymer-aerogel composite coating can include a polymer and an ultra high water content catalyzed polysilicate aerogel, the polysilicate aerogel including a three dimensional network of silica particles having surface functional groups derivatized with a silylating agent and a plurality of pores.

  4. Durable polymer-aerogel based superhydrophobic coatings: a composite material

    DOEpatents

    Kissel, David J.; Brinker, Charles Jeffrey

    2016-02-02

    Provided are polymer-aerogel composite coatings, devices and articles including polymer-aerogel composite coatings, and methods for preparing the polymer-aerogel composite. The exemplary article can include a surface, wherein the surface includes at least one region and a polymer-aerogel composite coating disposed over the at least one region, wherein the polymer-aerogel composite coating has a water contact angle of at least about 140.degree. and a contact angle hysteresis of less than about 1.degree.. The polymer-aerogel composite coating can include a polymer and an ultra high water content catalyzed polysilicate aerogel, the polysilicate aerogel including a three dimensional network of silica particles having surface functional groups derivatized with a silylating agent and a plurality of pores.

  5. Confinement effects of polymers in porous glasses

    NASA Astrophysics Data System (ADS)

    Crupi, V.; Majolino, D.; Migliardo, P.; Venuti, V.

    1998-07-01

    Recently, confinement effects on dynamical properties of liquids inside restricted volumes have been extensively studied, either from a theoretical or technological point of view, thanks to the large possibility of industrial applications (building of optical switches, membrane separation, catalysis). We performed depolarized light scattering measurements on propylene glycol (PG) and its oligomers poly(propylene glycols) (PPG) having different molecular weights ( Mw, 425, 725 and 4000 Da), in the bulk state and confined in a silica glass having 25 Å pores. Mainly, two relevant effects are responsible for the dynamical response of liquids that diffuse and reorient in a confined geometry: (a) the 'physical traps', related to both dead-end groups and the tortuosity of the percolated channels for diffusion; and (b) the 'chemical traps', related to the degree of the absorption of molecules on the active surface sites. Hence, by comparing the behaviour of bulk polymers with confined polymers we were able to analyse the confinement influence on the molecular mobility of hydrogen-bonded liquids with different steric hindrance. The experimental results showed a frustration of molecular mobility in the confined samples owing to chemical and physical traps whose main role was highlighted thanks to the opportunity to substitute the active silanol groups (SiOH) in the inner surfaces with the non-active groups in the surfaces (treatment with methanol). In particular, we found that, in the case of low molecular weight samples, the relevant retardation process is connected to the chemical traps while for long chain polymers the physical traps play the main role. Further, the fitting procedure provided a distribution of relaxation times in the bulk systems and in short chain systems when confined in modified glass showing, in particular in the first case, that the distribution of relaxation times increases with polymers weights, occurrence related to a variety of molecular

  6. Durability of an inorganic polymer concrete coating

    NASA Astrophysics Data System (ADS)

    Wasserman, Kenneth

    The objective of the research program reported in this thesis is to evaluate the durability of an inorganic polymer composite coating exposed to freeze/thaw cycling and wet-dry cycling. Freeze/thaw cycling is performed following ASTM D6944-09 Standard Practice for Resistance of Cured Coatings to Thermal Cycling and wet/dry cycling is performed following guidelines set forth in a thesis written by Ronald Garon at Rutgers University. For both sets of experiments, four coating mixture proportions were evaluated. The variables were: silica/alumina ratio, mixing protocol using high shear and normal shear mixing, curing temperatures of 70 and 120 degrees Fahrenheit and use of nano size constituent materials. The mix with highest silica/alumina ratio was designated as Mix 1 and mixes with lower ratios were designated as Mix 2 and Mix 3. Mix 4 had nano silica particles. Four prisms were used for each variable including control that had no coating. The performance of the coating was evaluated using adhesion strength measured using: ASTM D7234 Test Method for Pull-Off Strength of Coatings on Concrete Using Portable Adhesion Testers. Tests were performed after every five consecutive cycles of thermal conditioning and six consecutive cycles of wet-dry exposure. Results from the thermal cycling and wet-dry testing demonstrate that all coating formulations are durable. The minimum adhesion strength was 300 psi even though a relatively weak base concrete surface was chosen for the study. The weak surface was chosen to simulate aged concrete surfaces present in actual field conditions. Due to the inherent nature of the test procedure the variation in test results is high. However, based on the test results, high shear mixer and high temperature curing are not recommended. As expected nano size constituent materials provide better performance.

  7. Tandem cylinder aerodynamic sound control using porous coating

    NASA Astrophysics Data System (ADS)

    Liu, Hanru; Azarpeyvand, Mahdi; Wei, Jinjia; Qu, Zhiguo

    2015-01-01

    This study is concerned with the application of porous coatings as a passive flow control method for reducing the aerodynamic sound from tandem cylinders. The aim here is to perform a parametric proof-of-concept study to investigate the effectiveness of porous treatment on bare tandem cylinders to control and regularize the vortex shedding and flow within the gap region between the two bluff bodies, and thereby control the aerodynamic sound generation mechanism. The aerodynamic simulations are performed using 2D transient RANS approach with k - ω turbulence model, and the acoustic computations are carried out using the standard Ffowcs Williams-Hawkings (FW-H) acoustic analogy. Numerical flow and acoustic results are presented for bare tandem cylinders and porous-covered cylinders, with different porosities and thicknesses. Experimental flow and acoustic data are also provided for comparison. Results show that the proper use of porous coatings can lead to stabilization of the vortex shedding within the gap region, reduction of the vortex shedding interaction with the downstream body, and therefore the generation of tonal and broadband noise. It has also been observed that the magnitude and the frequency of the primary tone reduce significantly as a result of the flow regularization. The proposed passive flow-induced noise and vibration control method can potentially be used for other problems involving flow interaction with bluff bodies.

  8. Carbon coatings on polymers and their biocompatibility

    NASA Astrophysics Data System (ADS)

    Hubáček, T.; Siegel, J.; Khalili, R.; Slepičková-Kasálková, N.; Švorčík, V.

    2013-06-01

    In this paper we modified the surface properties of polymer foils (polyethyleneterephthalate (PET) and polytetrafluoroethylene (PTFE)) by flash evaporation of carbon layers (C-layers). Adhesion and proliferation of vascular smooth muscle cells (VSMC) on carbon coated PTFE and PET were studied in vitro. Chemical composition of deposited C-layers was determined by Raman spectroscopy, surface contact angle was measured by goniometry. Surface morphology of carbon coated samples was studied using atomic force microscopy. Electrical properties of deposited C-layers were determined by measuring its sheet resistance. It was found that the carbon deposition leads to a decrease of surface roughness of PTFE and PET and to a significant increase of sample wettability. Electrical resistance and wettability of deposited C-layers depends significantly on both the thickness of C-layer and the type of polymeric substrate used. It was found that maximal stimulation of the VSMC (adhesion and proliferation) on carbon coated polymers depends on the surface roughness and contact angle of cell carriers used.

  9. Hemocompatible, pulsed laser deposited coatings on polymers.

    PubMed

    Lackner, Juergen M; Waldhauser, Wolfgang; Major, Roman; Major, Boguslaw; Bruckert, Franz

    2010-02-01

    State-of-the-art non-thrombogenic blood contacting surfaces are based on heparin and struggle with the problem of bleeding. However, appropriate blood flow characteristics are essential for clinical application. Thus, there is increasing demand to develop new coating materials for improved human body acceptance. Materials deposited by vacuum coating techniques would be an excellent alternative if the coating temperatures can be kept low because of the applied substrate materials of low temperature resistance (polymers). Most of the recently used plasma-based deposition techniques cannot fulfill this demand. However, adequate film structure and high adhesion can be reached by the pulsed laser deposition at room temperature, which was developed to an industrial-scaled process at Laser Center Leoben. Here, this process is described in detail and the resulting structural film properties are shown for titanium, titanium nitride, titanium carbonitride, and diamond-like carbon on polyurethane, titanium and silicon substrates. Additionally, we present the biological response of blood cells and the kinetic mechanism of eukaryote cell attachment. In conclusion, high biological acceptance and distinct differences for the critical delamination shear stress were found for the coatings, indicating higher adhesion at higher carbon contents. PMID:20128746

  10. Porous light-emitting compositions

    DOEpatents

    Burrell, Anthony K.; McCleskey, Thomas Mark; Jia, Quanxi; Bauer, Eve; Mueller, Alexander H.

    2012-04-17

    Light-emitting devices are prepared by coating a porous substrate using a polymer-assisted deposition process. Solutions of metal precursor and soluble polymers having binding properties for metal precursor were coated onto porous substrates. The coated substrates were heated at high temperatures under a suitable atmosphere. The result was a substrate with a conformal coating that did not substantially block the pores of the substrate.

  11. Protection of alodine coatings from thermal aging by removable polymer coatings.

    SciTech Connect

    Wagstaff, Brett R.; Bradshaw, Robert W.; Whinnery, LeRoy L., Jr.

    2006-12-01

    Removable polymer coatings were evaluated as a means to suppress dehydration of Alodine chromate conversion coatings during thermal aging and thereby retain the corrosion protection afforded by Alodine. Two types of polymer coatings were applied to Alodine-treated panels of aluminum alloys 7075-T73 and 6061-T6 that were subsequently aged for 15 to 50 hours at temperatures between 135 F to 200 F. The corrosion resistance of the thermally aged panels was evaluated, after stripping the polymer coatings, by exposure to a standard salt-fog corrosion test and the extent of pitting of the polymer-coated and untreated panels compared. Removable polymer coatings mitigated the loss of corrosion resistance due to thermal aging experienced by the untreated alloys. An epoxide coating was more effective than a fluorosilicone coating as a dehydration barrier.

  12. Corrosion-protective coatings from electrically conducting polymers

    SciTech Connect

    Thompson, K.G.; Bryan, C.J.; Benicewicz, B.C.; Wrobleski, D.A.

    1991-12-31

    In a joint research effort involving the Kennedy Space Center and the Los Alamos National Laboratory, electrically conductive polymer coatings have been developed as corrosion-protective coatings for metal surfaces. At the Kennedy Space Center, the launch environment consists of marine, severe solar, and intermittent high acid/elevated temperature conditions. Electrically conductive polymer coatings have been developed which impart corrosion resistance to mild steel when exposed to saline and acidic environments. Such coatings also seem to promote corrosion resistance in areas of mild steel where scratches exist in the protective coating. Such coatings appear promising for many commercial applications.

  13. Corrosion-protective coatings from electrically conducting polymers

    NASA Technical Reports Server (NTRS)

    Thompson, Karen Gebert; Bryan, Coleman J.; Benicewicz, Brian C.; Wrobleski, Debra A.

    1991-01-01

    In a joint effort between NASA Kennedy and LANL, electrically conductive polymer coatings were developed as corrosion protective coatings for metal surfaces. At NASA Kennedy, the launch environment consist of marine, severe solar, and intermittent high acid and/or elevated temperature conditions. Electrically conductive polymer coatings were developed which impart corrosion resistance to mild steel when exposed to saline and acidic environments. Such coatings also seem to promote corrosion resistance in areas of mild steel where scratches exist in the protective coating. Such coatings appear promising for many commercial applications.

  14. Adsorption of acenaphthene on porous organic polymers

    SciTech Connect

    Eichenmueller, B.; Bunke, G.; Buchholz, R.; Goetz, P.; Behrend, K.

    1997-09-01

    Adsorption behavior of the three-ring polynuclear aromatic hydrocarbon (PAH) acenaphthene from aqueous solutions on the adsorber polymers Wofatit EP 61 and EP 63 was examined. Using dimethylsulfoxide as a solubilizer, equilibrium, kinetic, and fixed-bed dynamic experiments could be carried out. Freundlich parameters for equilibrium data were obtained, exhibiting high capacities at low liquid concentrations: K{sub F} = 0.14 mg{sup 1{minus}n} {center_dot} L{sup n}/mg{sub A} and n = 0.5 for EP 61; and K{sub F} = 0.22 mg{sup 1{minus}n} {center_dot} L/mg{sub A} and n = 0.39 for EP 63. By fitting the numerical solution of a mathematical model to experimental data from kinetic experiments in a differential bed adsorber operated at high circulation velocity, effective intraparticle diffusivity could be estimated to be D{sub eff} = 2.5 {center_dot} 10{sup {minus}10} cm{sup 2}/s. According to these data and parameters from empirical equations, breakthrough curves were predicted analytically and numerically and compared to experimental data. A good agreement with the numerical solution was observed. The presence of dimethylsulfoxide influenced neither equilibrium nor kinetic data.

  15. Preparation and Performance of Plasma/Polymer Composite Coatings on Magnesium Alloy

    NASA Astrophysics Data System (ADS)

    Bakhsheshi-Rad, H. R.; Hamzah, E.; Bagheriyan, S.; Daroonparvar, M.; Kasiri-Asgarani, M.; Shah, A. M.; Medraj, M.

    2016-07-01

    A triplex plasma (NiCoCrAlHfYSi/Al2O3·13%TiO2)/polycaprolactone composite coating was successfully deposited on a Mg-1.2Ca alloy by a combination of atmospheric plasma spraying and dip-coating techniques. The NiCoCrAlHfYSi (MCrAlHYS) coating, as the first layer, contained a large number of voids, globular porosities, and micro-cracks with a thickness of 40-50 μm, while the Al2O3·13%TiO2 coating, as the second layer, presented a unique bimodal microstructure with a thickness of 70-80 μm. The top layer was a hydrophobic polymer, which effectively sealed the porosities of plasma layers. The results of micro-hardness and bonding strength tests showed that the plasma coating presented excellent hardness (870 HV) and good bonding strength (14.8 MPa). However, the plasma/polymer coatings interface exhibited low bonding strength (8.6 MPa). The polymer coating formed thick layer (100-110 μm) that homogeneously covered the surface of the plasma layers. Contact angle measurement showed that polymer coating over plasma layers significantly decreased surface wettability. The corrosion current density (i corr) of an uncoated sample (262.7 µA/cm2) decreased to 76.9 µA/cm2 after plasma coatings were applied. However, it was found that the i corr decreased significantly to 0.002 µA/cm2 after polymer sealing of the porous plasma layers.

  16. Stable low-fouling plasma polymer coatings on polydimethylsiloxane

    PubMed Central

    Forster, S.; McArthur, S. L.

    2012-01-01

    Polydimethylsiloxane (DMS) is a popular material for microfluidics, but it is hydrophobic and is prone to non-specific protein adsorption. In this study, we explore methods for producing stable, protein resistant, tetraglyme plasma polymer coatings on PDMS by combining extended baking processes with multiple plasma polymer coating steps. We demonstrate that by using this approach, it is possible to produce a plasma polymer coatings that resist protein adsorption (<10 ng/cm2) and are stable to storage over at least 100 days. This methodology can translate to any plasma polymer system, enabling the introduction of a wide range of surface functionalities on PDMS surfaces. PMID:24062864

  17. Corrosion protection performance of porous strontium hydroxyapatite coating on polypyrrole coated 316L stainless steel.

    PubMed

    Gopi, D; Ramya, S; Rajeswari, D; Kavitha, L

    2013-07-01

    Polypyrrole/strontium hydroxyapatite bilayer coatings were achieved on 316L stainless steel (316L SS) by the electropolymerisation of pyrrole from sodium salicylate solution followed by the electrodeposition of porous strontium hydroxyapatite. The formation and the morphology of the bilayer coatings were characterised by Fourier transform infrared spectroscopy (FT-IR) and high resolution scanning electron microscopy (HRSEM), respectively. The corrosion resistance of the coated 316L SS specimens was investigated in Ringer's solution by electrochemical techniques and the results were substantiated with inductively coupled plasma atomic emission spectrometry (ICP-AES). The passive film underneath the polypyrrole layer is effective in protecting 316L SS against corrosion in Ringer's solution. Moreover, we believe that the top porous strontium hydroxyapatite layer can provide potential bioactivity to the 316L SS. PMID:23475060

  18. Multilayered Polymer Coated Carbon Nanotubes to Deliver Dasatinib

    PubMed Central

    Moore, Thomas L.; Grimes, Stuart W.; Lewis, Robert L.; Alexis, Frank

    2014-01-01

    Multilayered, multifunctional polymer coatings were grafted onto carbon nanotubes (CNT) using a one-pot, ring-opening polymerization in order to control the release kinetic and therapeutic efficacy of dasatinib. Biocompatible, biodegradable multilayered coatings composed of poly(glycolide) (PGA), and poly(lactide) (PLA) were polymerized directly onto hydroxyl-functionalized CNT surfaces. Sequential addition of monomers into the reaction vessel enabled multilayered coatings of PLA-PGA, or PGA-PLA. Poly(ethylene glycol) capped the polymer chain ends, resulting in a multifunctional amphiphilic coating. Multilayer polymer coatings on CNTs enabled control of anticancer dasatinib’s release kinetics and enhanced the in vitro therapeutic efficacy against U-87 glioblastoma compared to monolayer polymer coatings. PMID:24294824

  19. Modeling Methane Adsorption in Interpenetrating Porous Polymer Networks

    SciTech Connect

    Martin, RL; Shahrak, MN; Swisher, JA; Simon, CM; Sculley, JP; Zhou, HC; Smit, B; Haranczyk, M

    2013-10-03

    Porous polymer networks (PPNs) are a class of porous materials of particular interest in a variety of energy-related applications because of their stability, high surface areas, and gas uptake capacities. Computationally derived structures for five recently synthesized PPN frameworks, PPN-2, -3, -4, -5, and -6, were generated for various topologies, optimized using semiempirical electronic structure methods, and evaluated using classical grand canonical Monte Carlo simulations. We show that a key factor in modeling the methane uptake performance of these materials is whether, and how, these material frameworks interpenetrate and demonstrate a computational approach for predicting the presence, degree, and nature of interpenetration in PPNs that enables the reproduction of experimental adsorption data.

  20. New Polymer Coatings for Chemically Selective Mass Sensors

    NASA Technical Reports Server (NTRS)

    Sims, S. C.; Wright, Cassandra; Cobb, J.; McCalla, T.; Revelle, R.; Morris, V. R.; Pollack, S. K.

    1997-01-01

    There is a current need to develop sensitive and chemically specific sensors for the detection of nitric acid for in-situ measurements in the atmosphere. Polymer coatings have been synthesized and tested for their sensitivity and selectivity to nitric acid. A primary requirement for these polymers is detectability down to the parts per trillion range. The results of studies using these polymers as coatings for quartz crystal microbalances (QCM) and surface acoustic wave (SAW) devices will be presented.

  1. The Evaluation of Hydroxyapatite (HA) Coated and Uncoated Porous Tantalum for Biomedical Material Applications

    NASA Astrophysics Data System (ADS)

    Safuan, Nadia; Sukmana, Irza; Kadir, Mohammed Rafiq Abdul; Noviana, Deni

    2014-04-01

    Porous tantalum has been used as an orthopedic implant for bone defects as it has a good corrosion resistance and fatigue behaviour properties. However, there are some reports on the rejection of porous Ta after the implantation. Those clinical cases refer to the less bioactivity of metallic-based materials. This study aims to evaluate hydroxyapatite coated and uncoated porous Tantalum in order to improve the biocompatibility of porous tantalum implant and osseointegration. Porous tantalum was used as metallic-base substrate and hydroxyapatite coating has been done using plasma-spraying technique. Scanning Electron Microscopy (SEM) and Field Emission Scanning Electron Microscopy (FESEM) techniques were utilizes to investigate the coating characteristics while Confocal Raman Microscopy to investigate the interface and image. The effect of coating to the corrosion behaviour was assessed by employing potentiodynamic polarization tests in simulated body fluid at 37±1 °C. Based on SEM and FESEM results, the morphologies as well the weight element consists in the uncoated and hydroxyapatite coated porous tantalum were revealed. The results indicated that the decrease in corrosion current density for HA coated porous Ta compared to the uncoated porous Ta. This study concluded that by coating porous tantalum with HA supports to decrease the corrosion rate of pure porous.

  2. Conductive polymer coatings for anodes in aqueous electrowinning

    NASA Astrophysics Data System (ADS)

    Alfantazi, A. M.; Moskalyk, R. R.

    2003-07-01

    This article discusses the potential application of electrically conductive polymers as protective coatings for permanent lead anodes employed in aqueous electrowinning processes. Also presented are results from a preliminary study of the performance of two intrinsically conductive polymers (polyaniline and poly 3,4,5-trifluorophenylthiophene [TFPT]) under mild copper electrowinning conditions as conductive and protective coatings on anodic surfaces. The laboratory results indicated that using lead alloy anodes coated with TFPT merits continued research.

  3. Biodegradable polymer for sealing porous PEO layer on pure magnesium: An in vitro degradation study

    NASA Astrophysics Data System (ADS)

    Alabbasi, Alyaa; Mehjabeen, Afrin; Kannan, M. Bobby; Ye, Qingsong; Blawert, Carsten

    2014-05-01

    An attempt was made to seal the porous silicate-based plasma electrolytic oxidation (PEO) layer on pure magnesium (Mg) with a biodegradable polymer, poly(L-lactide) (PLLA), to delay the localized degradation of magnesium-based implants in body fluid for better in-service mechanical integrity. Firstly, a silicate-based PEO coating on pure magnesium was performed using a pulsed constant current method. In order to seal the pores in the PEO layer, PLLA was coated using a two-step spin coating method. The performance of the PEO-PLLA Mg was evaluated using electrochemical impedance spectroscopy (EIS) and potentiodynamic polarization. The EIS results showed that the polarization resistance (Rp) of the PEO-PLLA Mg was close to two orders of magnitude higher than that of the PEO Mg. While the corrosion current density (icorr) of the pure Mg was reduced by 65% with the PEO coating, the PEO-PLLA coating reduced the icorr by almost 100%. As expected, the Rp of the PEO-PLLA Mg decreased with increase in exposure time. However, it was noted that the Rp of the PEO-PLLA Mg even after 100 h was six times higher than that of the PEO Mg after 48 h exposure, and did not show any visible localized attack.

  4. Cysteine could change the transport mechanism of PVP-coated silver nanoparticles in porous media

    NASA Astrophysics Data System (ADS)

    Yang, X.; Lin, S.; Wiesner, M.

    2012-12-01

    Silver nanoparticles (AgNPs) can hardly be removed by wastewater treatment plant and have big potential to enter groundwater, jeopardizing the water quality & aquatic ecosystem. Most AgNPs have surface coatings such as polyvinylpyrrolidone (PVP) which dominate their transport in porous media. Our previous study shows that PVP may promote the deposition of AgNPs on silica surface by a bridging mechanism. This study further explored how cysteine, a natural organic matter type, may influence the role of the PVP coating on AgNP translocation. Dynamic Light Scattering (DLS) measurement (Figure 1A) shows that the PVP coating rendered the AgNP dispersion high stability during the measuring period (3hrs). Addition of 100 ppm cysteine to the dispersion resulted in a rapid decrease in particle size from 100nm to 52nm within one hour, following which no further decline in particle size occurred. Column experiment results (Figure 1B) show that corresponding to the particle size change was a substantial decrease in particle deposition rates: introduction of 100 ppm cysteine into the particle dispersion resulted in a decrease in AgNP attenuation by the porous medium from 67% to 26%. The decline in particle size suggested that cysteine may have displaced the macromolecular PVP from the particle surface. Desorption of PVP resulted in a weakening or vanish of polymer bridging effect which in turn lowered the deposition rates substantially. This study demonstrated an implication of environmental transformation of coated AgNPs to their mobility in saturated sand aquifers. Acknowledgment Xinyao Yang appreciates the Natural Science Foundation of China (Grant No.:41101475) for covering the registration fee and traveling costs.igure 1 Particle size measurement (A) and breakthrough curves (B) of PVP-coated silver nanoparticle in the absence and presence of cysteine: pH=7.0, ionic strength=1mM, flow rate=1ml/min.

  5. Influence of relative humidity during coating on polymer deposition and film formation.

    PubMed

    Macchi, Elena; Felton, Linda A

    2016-08-20

    The influence of relative humidity in the pan during coating on polymer deposition and film formation was investigated. Four tablet substrates, differing in hydrophobicity, porosity, and surface roughness, were prepared and coated with Eudragit(®) RS/RL 30 D (8:2 ratio). The spray rate and atomization air pressure were varied to create two distinct micro-environmental conditions in the coating pan. PyroButton data logging devices placed directly in the pan were found to more accurately reflect the relative humidity to which tablets were exposed in comparison to measurements taken at the exhaust. Polymer deposition was shown to be influenced by the properties of the substrate, rather than the processing conditions used during coating, with higher polymer weight gains observed for the more porous tablets. Differences in the film-tablet interface and in the release performance of the coated products, however, were attributed to both the relative humidity in the pan and tablet porosity. Overall, this study demonstrated that a more humid coating process (86% vs 67%) promoted surface dissolution and physical mixing of the tablet ingredients with the forming film and the extent of this phenomenon was dependent on the tablet porosity. PMID:27282533

  6. Characterization of Porous, Dexamethasone-Releasing Polyurethane Coatings for Glucose Sensors

    PubMed Central

    Vallejo-Heligon, Suzana G.; Klitzman, Bruce; Reichert, William M.

    2014-01-01

    Commercially available implantable needle-type glucose sensors for diabetes management are robust analytically but can be unreliable clinically primarily due to tissue-sensor interactions. Here, we present the physical, drug release, and bioactivity characterization of tubular, porous dexamethasone (Dex) releasing polyurethane coatings designed to attenuate local inflammation in the tissue-sensor interface. Porous polyurethane coatings were produced by the salt-leaching/gas-foaming method. Scanning electron microscopy (SEM) and Micro-computed tomography (Micro-CT) showed a controlled porosity and coating thickness. In vitro drug release from coatings monitored over two weeks presented an initial fast release followed by a slower release. Total release from coatings was highly dependent on initial drug loading amount. Functional in vitro testing of glucose sensors deployed with porous coatings against glucose standards demonstrated that highly porous coatings minimally affected signal strength and response rate. Bioactivity of the released drug was determined by monitoring Dex-mediated, dose-dependent apoptosis of human peripheral blood derived monocytes in culture. Acute animal studies were used to determine the appropriate Dex payload for the implanted porous coatings. Pilot short-term animal studies showed that Dex released from porous coatings implanted in rat subcutis attenuated the initial inflammatory response to sensor implantation. These results suggest that deploying sensors with the porous, Dex-releasing coatings is a promising strategy to improve glucose sensor performance. PMID:25065548

  7. Characterization of porous, dexamethasone-releasing polyurethane coatings for glucose sensors.

    PubMed

    Vallejo-Heligon, Suzana G; Klitzman, Bruce; Reichert, William M

    2014-11-01

    Commercially available implantable needle-type glucose sensors for diabetes management are robust analytically but can be unreliable clinically primarily due to tissue-sensor interactions. Here, we present the physical, drug release and bioactivity characterization of tubular, porous dexamethasone (Dex)-releasing polyurethane coatings designed to attenuate local inflammation at the tissue-sensor interface. Porous polyurethane coatings were produced by the salt-leaching/gas-foaming method. Scanning electron microscopy and micro-computed tomography (micro-CT) showed controlled porosity and coating thickness. In vitro drug release from coatings monitored over 2 weeks presented an initial fast release followed by a slower release. Total release from coatings was highly dependent on initial drug loading amount. Functional in vitro testing of glucose sensors deployed with porous coatings against glucose standards demonstrated that highly porous coatings minimally affected signal strength and response rate. Bioactivity of the released drug was determined by monitoring Dex-mediated, dose-dependent apoptosis of human peripheral blood derived monocytes in culture. Acute animal studies were used to determine the appropriate Dex payload for the implanted porous coatings. Pilot short-term animal studies showed that Dex released from porous coatings implanted in rat subcutis attenuated the initial inflammatory response to sensor implantation. These results suggest that deploying sensors with the porous, Dex-releasing coatings is a promising strategy to improve glucose sensor performance. PMID:25065548

  8. Stability analysis of a polymer coating process

    NASA Astrophysics Data System (ADS)

    Kallel, A.; Hachem, E.; Demay, Y.; Agassant, J. F.

    2015-05-01

    A new coating process involving a short stretching distance (1 mm) and a high draw ratio (around 200) is considered. The resulting thin molten polymer film (around 10 micrometers) is set down on a solid primary film and then covered by another solid secondary film. In experimental studies, periodical fluctuation in the thickness of the coated layer may be observed. The processing conditions markedly influence the onset and the development of these defects and modeling will help our understanding of their origins. The membrane approach which has been commonly used for cast film modeling is no longer valid and two dimensional time dependent models (within the thickness) are developed in the whole domain (upstream die and stretching path). A boundary-value problem with a free surface for the Stokes equations is considered and stability of the free surface is assessed using two different numerical strategies: a tracking strategy combined with linear stability analysis involving computation of leading eigenvalues, and a Level Set capturing strategy coupled with transient stability analysis.

  9. Photothermally responsive gold nanoparticle conjugated polymer-grafted porous hollow silica nanocapsules.

    PubMed

    Paramelle, David; Gorelik, Sergey; Liu, Ye; Kumar, Jatin

    2016-08-01

    Polymer-grafted porous hollow silica nanoparticles prepared by reversible addition-fragmentation chain transfer polymerisation have an upper critical solution temperature of 45 °C. Conjugation of 5 nm gold nanoparticles onto polymer-grafted porous hollow silica nanoparticles enables remarkable specific photothermally-induced controlled release of encapsulated Rhodamine B by laser-stimulation at physiological temperature. PMID:27427407

  10. Synthesis and characterization of porous hydroxyapatite and hydroxyapatite coatings

    SciTech Connect

    Nieh, T G; Choi, B W; Jankowski, A F

    2000-10-25

    A technique is developed to construct bulk hydroxyapatite (HAp) with different cellular structures. The technique involves the initial synthesis of nanocrystalline hydroxyapatite powder from an aqueous solution using water-soluble compounds and then followed by spray drying into agglomerated granules. The granules were further cold pressed and sintered into bulks at elevated temperatures. The sintering behavior of the HAp granules was characterized and compared with those previously reported. Resulting from the fact that the starting HAp powders were extremely fine, a relatively low activation energy for sintering was obtained. In the present study, both porous and dense structures were produced by varying powder morphology and sintering parameters. Porous structures consisting of open cells were constructed. Sintered structures were characterized using scanning electron microscopy and x-ray tomography. In the present paper, hydroxyapatite coatings produced by magnetron sputtering on silicon and titanium substrates will also be presented. The mechanical properties of the coatings were measured using nanoindentation techniques and microstructures examined using transmission electron microscopy.

  11. Porous polymer electrolytes with high ionic conductivity and good mechanical property for rechargeable batteries

    NASA Astrophysics Data System (ADS)

    Liang, Bo; Jiang, Qingbai; Tang, Siqi; Li, Shengliang; Chen, Xu

    2016-03-01

    Porous polymer electrolytes (PPEs) are attractive for developing lithium-ion batteries because of the combined advantages of liquid and solid polymer electrolytes. In the present study, a new porous polymer membrane doped with phytic acid (PA) is prepared, which is used as a crosslinker in polymer electrolyte matrix and can also plasticize porous polymer electrolyte membranes, changing them into soft tough flexible materials. A PEO-PMMA-LiClO4-x wt.% PA (x = weight of PA/weight of polymer, PEO: poly(ethylene oxide); PMMA: poly(methyl methacrylate)) polymer membrane is prepared by a simple evaporation method. The effects of the ratio of PA to PEO-PMMA on the properties of the porous membrane, including morphology, porous structure, and mechanical property, are systematically studied. PA improves the porous structure and mechanical properties of polymer membrane. The maximum tensile strength and elongation of the porous polymer membranes are 20.71 MPa and 45.7% at 15 wt.% PA, respectively. Moreover, the PPEs with 15 wt.% PA has a conductivity of 1.59 × 10-5 S/cm at 20 °C, a good electrochemical window (>5 V), and a low interfacial resistance. The results demonstrate the compatibility of the mechanical properties and conductivity of the PPEs, indicating that PPEs have good application prospects for lithium-ion batteries.

  12. Poly-ε-caprolactone Coated and Functionalized Porous Titanium and Magnesium Implants for Enhancing Angiogenesis in Critically Sized Bone Defects

    PubMed Central

    Roland, Laura; Grau, Michael; Matena, Julia; Teske, Michael; Gieseke, Matthias; Kampmann, Andreas; Beyerbach, Martin; Murua Escobar, Hugo; Haferkamp, Heinz; Gellrich, Nils-Claudius; Nolte, Ingo

    2015-01-01

    For healing of critically sized bone defects, biocompatible and angiogenesis supporting implants are favorable. Murine osteoblasts showed equal proliferation behavior on the polymers poly-ε-caprolactone (PCL) and poly-(3-hydroxybutyrate)/poly-(4-hydroxybutyrate) (P(3HB)/P(4HB)). As vitality was significantly better for PCL, it was chosen as a suitable coating material for further experiments. Titanium implants with 600 µm pore size were evaluated and found to be a good implant material for bone, as primary osteoblasts showed a vitality and proliferation onto the implants comparable to well bottom (WB). Pure porous titanium implants and PCL coated porous titanium implants were compared using Live Cell Imaging (LCI) with Green fluorescent protein (GFP)-osteoblasts. Cell count and cell covered area did not differ between the implants after seven days. To improve ingrowth of blood vessels into porous implants, proangiogenic factors like Vascular Endothelial Growth Factor (VEGF) and High Mobility Group Box 1 (HMGB1) were incorporated into PCL coated, porous titanium and magnesium implants. An angiogenesis assay was performed to establish an in vitro method for evaluating the impact of metallic implants on angiogenesis to reduce and refine animal experiments in future. Incorporated concentrations of proangiogenic factors were probably too low, as they did not lead to any effect. Magnesium implants did not yield evaluable results, as they led to pH increase and subsequent cell death. PMID:26703586

  13. Poly-ε-caprolactone Coated and Functionalized Porous Titanium and Magnesium Implants for Enhancing Angiogenesis in Critically Sized Bone Defects.

    PubMed

    Roland, Laura; Grau, Michael; Matena, Julia; Teske, Michael; Gieseke, Matthias; Kampmann, Andreas; Beyerbach, Martin; Murua Escobar, Hugo; Haferkamp, Heinz; Gellrich, Nils-Claudius; Nolte, Ingo

    2016-01-01

    For healing of critically sized bone defects, biocompatible and angiogenesis supporting implants are favorable. Murine osteoblasts showed equal proliferation behavior on the polymers poly-ε-caprolactone (PCL) and poly-(3-hydroxybutyrate)/poly-(4-hydroxybutyrate) (P(3HB)/P(4HB)). As vitality was significantly better for PCL, it was chosen as a suitable coating material for further experiments. Titanium implants with 600 µm pore size were evaluated and found to be a good implant material for bone, as primary osteoblasts showed a vitality and proliferation onto the implants comparable to well bottom (WB). Pure porous titanium implants and PCL coated porous titanium implants were compared using Live Cell Imaging (LCI) with Green fluorescent protein (GFP)-osteoblasts. Cell count and cell covered area did not differ between the implants after seven days. To improve ingrowth of blood vessels into porous implants, proangiogenic factors like Vascular Endothelial Growth Factor (VEGF) and High Mobility Group Box 1 (HMGB1) were incorporated into PCL coated, porous titanium and magnesium implants. An angiogenesis assay was performed to establish an in vitro method for evaluating the impact of metallic implants on angiogenesis to reduce and refine animal experiments in future. Incorporated concentrations of proangiogenic factors were probably too low, as they did not lead to any effect. Magnesium implants did not yield evaluable results, as they led to pH increase and subsequent cell death. PMID:26703586

  14. Improved electrochemical performance of lithium iron phosphate in situ coated with hierarchical porous nitrogen-doped graphene-like membrane

    NASA Astrophysics Data System (ADS)

    zhang, Yue; Huang, Yudai; Wang, Xingchao; Guo, Yong; Jia, Dianzeng; Tang, Xincun

    2016-02-01

    LiFePO4 in situ coated with hierarchical porous nitrogen-doped graphene-like membrane (HPNGM) composite derived from a electrospun polymer membrane (EPM) precursor has been achieved for the first time. The N-doped graphene-like membrane which is in situ coating on LiFePO4 can provide a highly conductive layer, and the hierarchical porous structure facilitates Li+ transfer. The composite exhibits a high reversible capacity (171 mAh g-1 at 0.1 C), excellent high-rate capability and cycling stability. In addition to construct the traditional structure of nanofiber or nanowire, the EPM can also form graphene-like structure after annealing, which is a new application in constructing sheet structure by electrospinning.

  15. Development of visible and infrared electrochromic devices based on porous conducting polymers

    NASA Astrophysics Data System (ADS)

    Jin, Ilsup

    Two of the research topics carried out in this dissertation were related to electrochromic materials and devices. The conducting polymer, poly (3,4-ethylenedioxythiophene), known as PEDOT, was used as the electrochromic element in these studies. The first objective in the research was to develop methods for decreasing the optical switching times of the devices. Since optical switching times are mainly governed by the diffusion of charge compensating counterions through the electrochromic layer, a more porous structure is expected to enhance the switching kinetics by increasing counterion diffusion. We synthesized porous PEDOT films by a galvanostatic electropolymerization method using high current densities. The visible wavelength electrochromic devices made with these materials exhibited switching times of less than 100 milliseconds. This is substantially faster than the ˜1 second switching times obtained with non-porous devices and clearly establishes that porous conducting polymers are able to achieve faster switching kinetics. The second objective of this research was to fabricate electrochromic devices that were able to modulate infrared reflection in the 8 to 12 mum range. Upon doping the PEDOT, there was a substantial change in the refractive index of polymer layer which induced a large index mismatch with the substrate and produced high reflection from the substrate/polymer interface. The reflection modulation between the doped and undoped states was approximated using Fresnel's relation. The calculated values were in reasonable agreement with the experimental results. The anti-reflection coating on germanium minimized surface reflection and enabled us to achieve contrast ratios of greater than 5 between the doped and undoped states. The kinetics of infrared switching was also measured. The third topic investigated in this dissertation is related to the emerging scientific area in which biology is integrated with nanoscience. The research was based on the

  16. Oriented immobilization of proteins on grafted porous polymers

    NASA Astrophysics Data System (ADS)

    Carbajal, M. Laura; Smolko, Eduardo E.; Grasselli, Mariano

    2003-08-01

    The modification of polymers by radiation grafting has been utilized for several decades. The penetrability of gamma rays allows to modify the internal surfaces of porous materials retaining its mechanical properties. In recent years applications of these materials to obtain chromatographic supports and biocatalysts have been reported. In this work, we described the grafting of glycidyl methacrylate (GMA) onto a macroporous polysulfone polymer. Reproducible amount of grafting, from 10% to 60% was obtained by choosing favourable monomer concentration and gamma radiation doses from 6 kGy up. Afterwards, iminodiacetic acid (IDA) and amino phenyl arsine oxide (PAO) were covalently attached to the grafted polyGMA, in correspondence with the grafting degree. Later on, a recombinant histidin-patch thioredoxin protein (HP-rTrx) was immobilized onto this surface by two different ways, involving specific protein orientations. The first one involves an IDA-Ni 2+ complex and three HP-rTrx's histidines and the other one involves a co-ordination site between PAO and two proximal HP-rTrx's cysteines, which corresponds to the active site of the enzyme. Specific polyclonal antibodies recognize HP-rTrx on the polymer. Proper orientation of the protein was confirmed by HP-rTrx activity measurements. The described procedure allows the successful oriented immobilization of a protein onto a macroporous polysulfone material.

  17. Laser-induced porous graphene films from commercial polymers

    PubMed Central

    Lin, Jian; Peng, Zhiwei; Liu, Yuanyue; Ruiz-Zepeda, Francisco; Ye, Ruquan; Samuel, Errol L. G.; Yacaman, Miguel Jose; Yakobson, Boris I.; Tour, James M.

    2014-01-01

    Synthesis and patterning of carbon nanomaterials cost effectively is a challenge in electronic and energy storage devices. Here report a one-step, scalable approach for producing and patterning porous graphene films with 3-dimensional networks from commercial polymer films using a CO2 infrared laser. The sp3-carbon atoms are photothermally converted to sp2-carbon atoms by pulsed laser irradiation. The resulting laser-induced graphene (LIG) exhibits high electrical conductivity. The LIG can be readily patterned to interdigitated electrodes for in-plane microsupercapacitors with specific capacitances of >4 mF·cm−2 and power densities of ~9 mW·cm−2. Theoretical calculations partially suggest that enhanced capacitance may result from LIG’s unusual ultra-polycrystalline lattice of pentagon-heptagon structures. Combined with the advantage of one-step processing of LIG in air from commercial polymer sheets, which would allow the employment of a roll-to-roll manufacturing process, this technique provides a rapid route to polymer-written electronic and energy storage devices. PMID:25493446

  18. Laser-induced porous graphene films from commercial polymers.

    PubMed

    Lin, Jian; Peng, Zhiwei; Liu, Yuanyue; Ruiz-Zepeda, Francisco; Ye, Ruquan; Samuel, Errol L G; Yacaman, Miguel Jose; Yakobson, Boris I; Tour, James M

    2014-01-01

    The cost effective synthesis and patterning of carbon nanomaterials is a challenge in electronic and energy storage devices. Here we report a one-step, scalable approach for producing and patterning porous graphene films with three-dimensional networks from commercial polymer films using a CO2 infrared laser. The sp(3)-carbon atoms are photothermally converted to sp(2)-carbon atoms by pulsed laser irradiation. The resulting laser-induced graphene (LIG) exhibits high electrical conductivity. The LIG can be readily patterned to interdigitated electrodes for in-plane microsupercapacitors with specific capacitances of >4 mF cm(-2) and power densities of ~9 mW cm(-2). Theoretical calculations partially suggest that enhanced capacitance may result from LIG's unusual ultra-polycrystalline lattice of pentagon-heptagon structures. Combined with the advantage of one-step processing of LIG in air from commercial polymer sheets, which would allow the employment of a roll-to-roll manufacturing process, this technique provides a rapid route to polymer-written electronic and energy storage devices. PMID:25493446

  19. Dopamine/Silica Nanoparticle Assembled, Microscale Porous Structure for Versatile Superamphiphobic Coating.

    PubMed

    Li, Fang; Du, Miao; Zheng, Qiang

    2016-02-23

    Artificial superamphiphobic surfaces, which could repel both water and low surface tension organic liquids, have been limited to particular kinds of materials or surfaces thus far. In this work, a kind of microscale porous coating was developed. Taking dopamine and hydrophilic fumed silica nanoparticles as initial building blocks, microscale porous coating was constructed via ice templation. Polydopamine bound silica nanoparticles together to form a porous structure network and rendered the coating to have potential for further postfunctionalization. After two-step CVD, the microscale porous coating changes from superhydrophilic to superamphiphobic, exhibiting super-repellency to droplets with surface tension of 73-23 mN/m. The influences of concentration of initial dopamine, hydrophilic fumed silica nanoparticles, and dry conditions on the formation of the porous structure have been studied to optimize the conditions. Coatings with different pore sizes and pore heights have been fabricated to discover the relationship between the structure parameters and the repellency of the porous coatings. Only with optimal pore size and pore height can the porous coating display superamphiphobicity. Compared with nanoscale, the microscale structure favors the achievement of superamphiphobicity. Given the outstanding adhesive ability of polydopamine, the superamphiphobic coatings have been successfully applied to various materials including artificial materials and natural materials. PMID:26828414

  20. Polymer Coats Leads on Implantable Medical Device

    NASA Technical Reports Server (NTRS)

    2008-01-01

    Langley Research Center s Soluble Imide (LaRC-SI) was discovered by accident. While researching resins and adhesives for advanced composites for high-speed aircraft, Robert Bryant, a Langley engineer, noticed that one of the polymers he was working with did not behave as predicted. After putting the compound through a two-stage controlled chemical reaction, expecting it to precipitate as a powder after the second stage, he was surprised to see that the compound remained soluble. This novel characteristic ended up making this polymer a very significant finding, eventually leading Bryant and his team to win several NASA technology awards, and an "R&D 100" award. The unique feature of this compound is the way that it lends itself to easy processing. Most polyimides (members of a group of remarkably strong and incredibly heat- and chemical-resistant polymers) require complex curing cycles before they are usable. LaRC-SI remains soluble in its final form, so no further chemical processing is required to produce final materials, like thin films and varnishes. Since producing LaRC-SI does not require complex manufacturing techniques, it has been processed into useful forms for a variety of applications, including mechanical parts, magnetic components, ceramics, adhesives, composites, flexible circuits, multilayer printed circuits, and coatings on fiber optics, wires, and metals. Bryant s team was, at the time, heavily involved with the aircraft polymer project and could not afford to further develop the polymer resin. Believing it was worth further exploration, though, he developed a plan for funding development and submitted it to Langley s chief scientist, who endorsed the experimentation. Bryant then left the high-speed civil transport project to develop LaRC-SI. The result is an extremely tough, lightweight thermoplastic that is not only solvent-resistant, but also has the ability to withstand temperature ranges from cryogenic levels to above 200 C. The thermoplastic

  1. Preparation of silica nanospheres and porous polymer membranes with controlled morphologies via nanophase separation

    PubMed Central

    2012-01-01

    We successfully synthesized two different structures, silica nanospheres and porous polymer membranes, via nanophase separation, based on a sol–gel process. Silica sol, which was in situ polymerized from tetraorthosilicate, was used as a precursor. Subsequently, it was mixed with a polymer that was used as a matrix component. It was observed that nanophase separation occurred after the mixing of polymer with silica sol and subsequent evaporation of solvents, resulting in organizing various structures, from random network silica structures to silica spheres. In particular, silica nanospheres were produced by manipulating the mixing ratio of polymer to silica sol. The size of silica beads was gradually changed from micro- to nanoscale, depending on the polymer content. At the same time, porous polymer membranes were generated by removing the silica component with hydrofluoric acid. Furthermore, porous carbon membranes were produced using carbon source polymer through the carbonization process. PMID:22873570

  2. Hydroxyapatite-silver nanoparticles coatings on porous polyurethane scaffold.

    PubMed

    Ciobanu, Gabriela; Ilisei, Simona; Luca, Constantin

    2014-02-01

    The present paper is focused on a study regarding the possibility of obtaining hydroxyapatite-silver nanoparticle coatings on porous polyurethane scaffold. The method applied is based on a combined strategy involving hydroxyapatite biomimetic deposition on polyurethane surface using a Supersaturated Calcification Solution (SCS), combined with silver ions reduction and in-situ crystallization processes on hydroxyapatite-polyurethane surface by sample immersing in AgNO3 solution. The morphology, composition and phase structure of the prepared samples were characterized by scanning electron microscopy coupled with energy dispersive X-ray spectroscopy (SEM-EDX), X-ray diffraction (XRD), UV-Vis spectroscopy and X-ray photoelectron spectroscopy (XPS) measurements. The data obtained show that a layer of hydroxyapatite was deposited on porous polyurethane support and the silver nanoparticles (average size 34.71 nm) were dispersed among and even on the hydroxyapatite crystals. Hydroxyapatite/polyurethane surface acts as a reducer and a stabilizing agent for silver ions. The surface plasmon resonance peak in UV-Vis absorption spectra showed an absorption maximum at 415 nm, indicating formation of silver nanoparticles. The hydroxyapatite-silver polyurethane scaffolds were tested against Staphylococcus aureus and Escherichia coli and the obtained data were indicative of good antibacterial properties of the materials. PMID:24411349

  3. Hemispheric titanium porous coated acetabular component without screw fixation.

    PubMed

    Dorr, L D; Wan, Z; Cohen, J

    1998-06-01

    One hundred fifteen hips in 108 patients with primary total hip arthroplasty using the anatomic porous replacement hemispheric acetabular component implanted without adjunctive screw fixation had a mean postoperative followup time of 6 years (range, 5-7.4 years). Clinical evaluation was performed using the Harris hip score and patient self assessment using a modified Short Form-36 questionnaire. Radiographs were measured for radiolucent lines, polyethylene wear, osteolysis, migration, and fractures. No acetabular metal shell had been revised for loosening or was radiographically loose with or without migration (more than 3 mm) at final followup. Reoperation was done in nine (8%) hips because of polyethylene insert wear or disassembly. No fracture of the acetabular bone occurred at the time of surgery or was observed on radiograph. Fixation of the metal shell was stable, with progressive radiolucent lines observed at final followup in 2% of the hips. Osteolysis was recorded in one patient with two acetabular components. The fixation of noncemented hemispheric porous coated acetabular components is more related to the technique of acetabular bone preparation and press fit implantation than to whether additional screws or peg fixation are used. Fixation of this acetabular component without screws at an average of 6 years after surgery is reproducible and predictable in primary hip arthroplasty. The design of modular polyethylene inserts has been improved and should reduce the wear rate of reoperations of the polyethylene insert. PMID:9646758

  4. Emulsion Templating Cyclic Polymers as Microscopic Particles with Tunable Porous Morphology.

    PubMed

    Wang, Dingguan; Xiao, Lifen; Zhang, Xinyue; Zhang, Ke; Wang, Yapei

    2016-02-16

    Cyclic polymers are a particular class of macromolecules without terminal groups. Most studies has involved their physical properties and polymer composition, while attention has rarely been paid to their emulsification in an oil-water system. Herein we synthesized a cyclic polymer with polystyrene side chains via ring-expansion metathesis polymerization and click-chemistry. This cyclic polymer was compared with linear polystyrene in order to investigate the effect of cyclic topology on preparing porous particles by emulsion templating methods. The contribution of cyclic topology to emulsification originates from the formation of hollow microspheres with the use of cyclic polymer while linear polymer only afforded solid microspheres. With addition of hexadecane as soft template, both cyclic polymer and linear polymer emulsions were successfully converted into porous particles. Superior to linear polymer, cyclic polymer enables the stabilization of emulsion droplets and the tuning of porous morphology. It is revealed that cyclic polymer with nanoring shape tends to assemble at the interfacial area, leading to the Pickering effect that decelerates the macrophase separation. Furthermore, the unique porous feature of polymer particles affords a convenient application for the detection of trace explosive. PMID:26799826

  5. Mussel-inspired antifouling coatings bearing polymer loops.

    PubMed

    Li, Lin; Yan, Bin; Zhang, Ling; Tian, Yu; Zeng, Hongbo

    2015-11-11

    This work reports the preparation of antifouling coatings bearing polymer loops using a mussel-inspired ABA triblock copolymer using a simple drop coating method. With similar end graft density, the loop-bearing surfaces show a more enhanced protein-reduction performance than the brush-bearing surfaces. PMID:26364998

  6. Preparation and characterization of beryllium doped organic plasma polymer coatings

    SciTech Connect

    Brusasco, R.; Letts, S.; Miller, P.; Saculla, M.; Cook, R.

    1995-10-04

    We report the formation of beryllium doped plasma polymerized coatings derived from a helical resonator deposition apparatus, using diethylberyllium as the organometaric source. These coatings had an appearance not unlike plain plasma polymer and were relatively stable to ambient exposure. The coatings were characterized by Inductively Coupled Plasma Mass Spectrometry and X-Ray Photoelectron Spectroscopy. Coating rates approaching 0.7 {mu}m hr{sup {minus}1} were obtained with a beryllium-to-carbon ratio of 1:1.3. There is also a significant oxygen presence in the coating as well which is attributed to oxidation upon exposure of the coating to air. The XPS data show only one peak for beryllium with the preponderance of the XPS data suggesting that the beryllium exists as BeO. Diethylberyllium was found to be inadequate as a source for beryllium doped plasma polymer, due to thermal decomposition and low vapor recovery rates.

  7. Polymer coated Capacitive Deionization Electrode for Desalination: A mini review

    NASA Astrophysics Data System (ADS)

    Gaikwad, Mahendra S.; Balomajumder, Chandrajit

    2016-02-01

    This mini review deals with a recently developing water purification technology, i.e. capacitive deionization. It presents the current progress achieved with polymer coated electrodes in capacitive deionization for desalination. The introduction covers capacitive deionization, application of polymer or polymer composite in capacitive deionization electrode, comparative study and discussion on fabrication of electrode. This paper aims at indicating novel research prospects in capacitive deionization technology for desalination.

  8. Apparatus for producing oxidation protection coatings for polymers

    NASA Technical Reports Server (NTRS)

    Mirtich, M. J. (Inventor); Sovey, J. S. (Inventor); Banks, A. (Inventor)

    1986-01-01

    A polymeric substrate is coated with a metal oxide film to provide oxidation protection in low Earth orbital environments. The film contains about 4 volume percent polymer to provide flexibility. A coil of polymer materials moves through an ion beam as it is fed between reels. The ion beam first cleans the polymer material surface and then sputters the film material from a target onto this surface.

  9. Apparatus and method for depositing coating onto porous substrate

    DOEpatents

    Isenberg, A.O.; Zymboly, G.E.

    1986-09-02

    Disclosed is an apparatus for forming a chemically vapor deposited coating on a porous substrate where oxygen from a first gaseous reactant containing a source of oxygen permeates through the pores of the substrate to react with a second gaseous reactant that is present on the other side of the substrate. The apparatus includes means for controlling the pressure and flow rate of each gaseous reactant, a manometer for measuring the difference in pressure between the gaseous reactants on each side of the substrate, and means for changing the difference in pressure between the gaseous reactants. Also disclosed is a method of detecting and closing cracks in the coating by reducing the pressure difference between the two gaseous reactants whenever the pressure difference falls suddenly after gradually rising, then again increasing the pressure difference on the two gases. The attack by the by-products of the reaction on the substrate are reduced by maintaining the flow rate of the first reactant through the pores of the substrate. 1 fig.

  10. Apparatus and method for depositing coating onto porous substrate

    DOEpatents

    Isenberg, Arnold O.; Zymboly, Gregory E.

    1986-01-01

    Disclosed is an apparatus for forming a chemically vapor deposited coating on a porous substrate where oxygen from a first gaseous reactant containing a source of oxygen permeates through the pores of the substrate to react with a second gaseous reactant that is present on the other side of the substrate. The apparatus includes means for controlling the pressure and flow rate of each gaseous reactant, a manometer for measuring the difference in pressure between the gaseous reactants on each side of the substrate, and means for changing the difference in pressure between the gaseous reactants. Also disclosed is a method of detecting and closing cracks in the coating by reducing the pressure difference between the two gaseous reactants whenever the pressure difference falls suddenly after gradually rising, then again increasing the pressure difference on the two gases. The attack by the by-products of the reaction on the substrate are reduced by maintaining the flow rate of the first reactant through the pores of the substrate.

  11. The influence of three-dimensional capillary-porous coatings on heat transfer at liquid boiling

    NASA Astrophysics Data System (ADS)

    Surtaev, A. S.; Pavlenko, A. N.; Kalita, V. I.; Kuznetsov, D. V.; Komlev, D. I.; Radyuk, A. A.; Ivannikov, A. Yu.

    2016-04-01

    The process of heat transfer at pool boiling of liquid (Freon R21) on tubes with three-dimensional plasma-deposited capillary-porous coatings of various thicknesses has been experimentally studied. Comparative analysis of experimental data showed that the heat transfer coefficient for a heater tube with a 500-μm-thick porous coating is more than twice as large as that in liquid boiling on an otherwise similar uncoated tube. At the same time, no intensification of heat exchange in the regime of bubble boiling is observed on a tube with a 100-μm-thick porous coating.

  12. Molecular Dynamics Simulations of Nanoparticles Coated with Charged Polymers

    NASA Astrophysics Data System (ADS)

    Wen, Chengyuan; Cheng, Shengfeng

    Polymer coating is frequently used to stabilize colloidal and nano-sized particles. We employ molecular dynamics simulations to study nanoparticles coated with polymer chains that contain ionizable groups. In a polar solvent, the chains become charged with counterions dissociated. In the computational model, we treat the solvent as a uniform dielectric background and use the bead-spring model for the polymer chains. Counterions are explicitly included as mobile beads. The nanoparticle is modeled as a layer of sites uniformly distributed on a spherical surface with a certain fraction of sites serving as the tether points of the grafted polymer brush. We vary the grafting density and calculate the distribution of polymer beads and counterions around the nanoparticle. Our results indicate that charged chains adopt extended conformations because of their mutual repulsions. We further study the interactions between two polymer-coated nanoparticles and obtain the potential of mean force. We also find an interesting transition of a confined single layer of such polymer-coated nanoparticles into two layers when the confinement is removed. Results show that the brush-brush contact has a nonuniform distribution and the nanoparticles tend to form dipole-like structures.

  13. Hierarchically porous polymers from hyper-cross-linked block polymer precursors.

    PubMed

    Seo, Myungeun; Kim, Soobin; Oh, Jaehoon; Kim, Sun-Jung; Hillmyer, Marc A

    2015-01-21

    We report synthesis of hierarchically porous polymers (HPPs) consisting of micropores and well-defined 3D continuous mesopores by combination of hyper-cross-linking and block polymer self-assembly. Copolymerization of 4-vinylbenzyl chloride (VBzCl) with divinylbenzene (DVB) in the presence of polylactide (PLA) macro-chain-transfer agent produced a cross-linked block polymer precursor PLA-b-P(VBzCl-co-DVB) via reversible addition-fragmentation chain transfer polymerization. A nanoscopic bicontinuous morphology containing PLA and P(VBzCl-co-DVB) microdomains was obtained as a result of polymerization-induced microphase separation. While a basic treatment of the precursor selectively removed PLA to yield a reticulated mesoporous polymer, hyper-cross-linking of the precursor by FeCl3 generated micropores in the P(VBzCl-co-DVB) microdomain via Friedel-Crafts alkylation and simultaneously degraded PLA to produce the HPP containing micropores in the mesoporous framework. The mesopore size of the HPP could be precisely controlled from 6 to 15 nm by controlling the molar mass of PLA. We demonstrate acceleration in adsorption rate in the HPP compared to a hyper-cross-linked microporous polymer. PMID:25551291

  14. Adsorption of anionic and cationic polymers on porous and non-porous calcium carbonate surfaces

    NASA Astrophysics Data System (ADS)

    Bjorklund, Robert B.; Arwin, Hans; Järnström, Lars

    1994-01-01

    The adsorption of anionic and cationic polymers onto calcium carbonate surfaces was studied by ellipsometry. Sodium polyacrylate was observed to both adsorb on and promote dissolution of polished limestone surfaces in 5 mM CaSO 4 solution at pH 10.3. It was not possible to differentiate between the two processes when they occurred simultaneously. Cationic starch adsorbed on the limestone surfaces at low concentrations and caused mineral dissolution at higher concentrations. The adsorbed amount of starch was higher on surfaces which were first made porous by partial dissolution than on freshly polished surfaces. Surfaces created by cleavage of Iceland spar calcite were quite stable against dissolution and the amount of starch adsorbed determined by ellipsometry agreed well with the adsorbed mass determined from batch adsorption experiments on ground calcite.

  15. In-syringe extraction using dissolvable layered double hydroxide-polymer sponges templated from hierarchically porous coordination polymers.

    PubMed

    Ghani, Milad; Frizzarin, Rejane M; Maya, Fernando; Cerdà, Víctor

    2016-07-01

    Herein we report the use of cobalt porous coordination polymers (PCP) as intermediates to prepare advanced extraction media based on layered double hydroxides (LDH) supported on melamine polymer foam. The obtained dissolvable Ni-Co LDH composite sponges can be molded and used as sorbent for the in-syringe solid-phase extraction (SPE) of phenolic acids from fruit juices. The proposed sorbent is obtained due to the surfactant-assisted self-assembly of Co(II)/imidazolate PCPs on commercially available melamine foam, followed by the in situ conversion of the PCP into the final dissolvable LDH coating. Advantageous features for SPE are obtained by using PCPs with hierarchical porosity (HPCPs). The LDH-sponge prepared using intermediate HPCPs (HLDH-sponge) is placed in the headspace of a glass syringe, enabling flow-through extraction followed by analyte elution by the dissolution of the LDH coating in acidic conditions. Three phenolic acids (gallic acid, p-hydroxybenzoic acid and caffeic acid) were extracted and quantified using high performance liquid chromatography. Using a 5mL sample volume, the obtained detection limits were 0.15-0.35μgL(-1). The proposed method for the preparation of HLDH-sponges showed a good reproducibility as observed from the intra- and inter-day RSD's, which were <10% for all analytes. The batch-to-batch reproducibility for three different batches of HLDH-sponges was 10.6-11.2%. Enrichment factors of 15-21 were obtained. The HLDH-sponges were applied satisfactorily to the determination of phenolic acids in natural and commercial fruit juices, obtaining relative recoveries among 89.7-95.3%. PMID:27247213

  16. Dual-Functional Antifogging/Antimicrobial Polymer Coating.

    PubMed

    Zhao, Jie; Ma, Li; Millians, William; Wu, Tiehang; Ming, Weihua

    2016-04-01

    Dual-functional antifogging/antimicrobial polymer coatings were prepared by forming a semi-interpenetrating polymer network (SIPN) of partially quaternized poly(2-(dimethylamino)ethyl methacrylate-co-methyl methacrylate) and polymerized ethylene glycol dimethacrylate network. The excellent antifogging behavior of the smooth coating was mainly attributed to the hydrophilic/hydrophobic balance of the partially quaternized copolymer, while the covalently bonded, hydrophobic quaternary ammonium compound (5 mol % in the copolymer) rendered the coating strongly antimicrobial, as demonstrated by the total kill against both Gram-positive Staphylococcus epidermidis and Gram-negative Escherichia coli. The antimicrobial action of the SIPN coating was based on contact killing, without leaching of bactericidal species, as revealed by a zone-of-inhibition test. This type of dual-functional coating may find unique applications where both antimicrobial and antifogging properties are desired. PMID:26977525

  17. Polymer coatings as separator layers for microbial fuel cell cathodes

    NASA Astrophysics Data System (ADS)

    Watson, Valerie J.; Saito, Tomonori; Hickner, Michael A.; Logan, Bruce E.

    2011-03-01

    Membrane separators reduce oxygen flux from the cathode into the anolyte in microbial fuel cells (MFCs), but water accumulation and pH gradients between the separator and cathode reduces performance. Air cathodes were spray-coated (water-facing side) with anion exchange, cation exchange, and neutral polymer coatings of different thicknesses to incorporate the separator into the cathode. The anion exchange polymer coating resulted in greater power density (1167 ± 135 mW m-2) than a cation exchange coating (439 ± 2 mW m-2). This power output was similar to that produced by a Nafion-coated cathode (1114 ± 174 mW m-2), and slightly lower than the uncoated cathode (1384 ± 82 mW m-2). Thicker coatings reduced oxygen diffusion into the electrolyte and increased coulombic efficiency (CE = 56-64%) relative to an uncoated cathode (29 ± 8%), but decreased power production (255-574 mW m-2). Electrochemical characterization of the cathodes ex situ to the MFC showed that the cathodes with the lowest charge transfer resistance and the highest oxygen reduction activity produced the most power in MFC tests. The results on hydrophilic cathode separator layers revealed a trade off between power and CE. Cathodes coated with a thin coating of anion exchange polymer show promise for controlling oxygen transfer while minimally affecting power production.

  18. Influence of biodegradable polymer coatings on corrosion, cytocompatibility and cell functionality of Mg-2.0Zn-0.98Mn magnesium alloy.

    PubMed

    Witecka, Agnieszka; Yamamoto, Akiko; Idaszek, Joanna; Chlanda, Adrian; Święszkowski, Wojciech

    2016-08-01

    Four kinds of biodegradable polymers were employed to prepare bioresorbable coatings on Mg-2.0Zn-0.98Mn (ZM21) alloy to understand the relationship between polymer characteristics, protective effects on substrate corrosion, cytocompatibility and cell functionality. Poly-l-lactide (PLLA), poly(3-hydroxybutyrate) (PHB), poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) or poly(lactic-co-glycolic) acid (PLGA) was spin-coated on ZM21, obtaining a smooth, non-porous coating less than 0.5μm in thickness. Polymer coating characterization, a degradation study, and biocompatibility evaluations were performed. After 4 w of immersion into cell culture medium, degradation of PLGA and PLLA coatings were confirmed by ATR-FTIR observation. The coatings of PLLA, PHB and PHBV, which have lower water permeability and slower degradation than PLGA, provide better suppression of initial ZM21 degradation and faster promotion of human osteosarcoma cell growth and differentiation. PMID:27100855

  19. Nanoparticle dispersion in disordered porous media with and without polymer additives.

    PubMed

    Babayekhorasani, Firoozeh; Dunstan, Dave E; Krishnamoorti, Ramanan; Conrad, Jacinta C

    2016-06-29

    In purely viscous Newtonian fluids, mechanical mixing of the fluid stream as it moves through an unstructured porous medium controls the long-time dispersion of molecular tracers. In applications ranging from environmental remediation to materials processing, however, particles are transported through porous media in polymer solutions and melts, for which the fluid properties depend on the shear rate and extent of deformation. How the flow characteristics of polymer solutions affect the spreading of finite-sized particles remains poorly understood - both on the microscopic scale as local velocity profiles, and on the macroscale as dispersion. Here, we show across a range of flow rates and disordered porous media configurations that the long-time transport coefficients of particles flowed in water, in a viscous Newtonian fluid, and in a non-Newtonian shear-thinning polymer solution collapse onto scaling curves, independent of the fluid rheology. Thus the addition of polymer does not impact nanoparticle dispersion through disordered porous media. PMID:27328208

  20. Boiling on horizontal surfaces coated with porous metal wicks

    SciTech Connect

    Abou-Zyan, H.Z.; Plumb, O.A.

    1997-07-01

    Boiling experiments intended to simulate heat pipe operating conditions were conducted on a copper surface covered with copper foametal and nickel fiber wicks 3.175 and 4.760 mm thick. The experiments were conducted on a horizontal surface open to the atmosphere with water as the working fluid. The experimental surface was operated like a heat pipe with distilled water supplied upstream of the heated section and transported by capillary action across a section which was adiabatic to the heated section where boiling took place. At low excess temperature, less than 10 to 20 C, the heat flux from the porous coated surfaces is comparable to or greater than that predicted for a smooth surface using the Rohsenow correlation. At higher excess temperatures corresponding to heat fluxes between 10{sup 5} and 10{sup 6} W/m{sup 2} the increase in heat flux with excess temperature is much less than that predicted by the Rohsenow correlation. When the wicks were vented by cutting slots covering 10 to 20% of the total surface area the heat flux increased, in some cases by a factor of three, for a given excess temperature. The heat flux at which the slope of the boiling curve decreased also increased for the vented surfaces. This is attributed to the provision of a low resistance path for the steam to escape providing a surface that is more highly wetted. A mathematical model for the transport with boiling in the porous wick is developed in an attempt to gain further understanding of the processes involved. The model predicts dryout conditions that are in reasonable agreement with experimental observations. However, the model predicts decreasing vapor pressure, and hence temperature, adjacent to the heated surface with increasing heat flux as a result of the decrease in relative permeability of the partially saturated wick.

  1. An instant multi-responsive porous polymer actuator driven by solvent molecule sorption

    NASA Astrophysics Data System (ADS)

    Zhao, Qiang; Dunlop, John W. C.; Qiu, Xunlin; Huang, Feihe; Zhang, Zibin; Heyda, Jan; Dzubiella, Joachim; Antonietti, Markus; Yuan, Jiayin

    2014-07-01

    Fast actuation speed, large-shape deformation and robust responsiveness are critical to synthetic soft actuators. A simultaneous optimization of all these aspects without trade-offs remains unresolved. Here we describe porous polymer actuators that bend in response to acetone vapour (24 kPa, 20 °C) at a speed of an order of magnitude faster than the state-of-the-art, coupled with a large-scale locomotion. They are meanwhile multi-responsive towards a variety of organic vapours in both the dry and wet states, thus distinctive from the traditional gel actuation systems that become inactive when dried. The actuator is easy-to-make and survives even after hydrothermal processing (200 °C, 24 h) and pressing-pressure (100 MPa) treatments. In addition, the beneficial responsiveness is transferable, being able to turn ‘inert’ objects into actuators through surface coating. This advanced actuator arises from the unique combination of porous morphology, gradient structure and the interaction between solvent molecules and actuator materials.

  2. Porous, High Capacity Coatings for Solid Phase Microextraction by Sputtering.

    PubMed

    Diwan, Anubhav; Singh, Bhupinder; Roychowdhury, Tuhin; Yan, DanDan; Tedone, Laura; Nesterenko, Pavel N; Paull, Brett; Sevy, Eric T; Shellie, Robert A; Kaykhaii, Massoud; Linford, Matthew R

    2016-02-01

    We describe a new process for preparing porous solid phase microextraction (SPME) coatings by the sputtering of silicon onto silica fibers. The microstructure of these coatings is a function of the substrate geometry and mean free path of the silicon atoms, and the coating thickness is controlled by the sputtering time. Sputtered silicon structures on silica fibers were treated with piranha solution (a mixture of concd H2SO4 and 30% H2O2) to increase the concentration of silanol groups on their surfaces, and the nanostructures were silanized with octadecyldimethylmethoxysilane in the gas phase. The attachment of this hydrophobic ligand was confirmed by X-ray photoelectron spectroscopy and contact angle goniometry on model, planar silicon substrates. Sputtered silicon coatings adhered strongly to their surfaces, as they were able to pass the Scotch tape adhesion test. The extraction time and temperature for headspace extraction of mixtures of alkanes and alcohols on the sputtered fibers were optimized (5 min and 40 °C), and the extraction performances of SPME fibers with 1.0 or 2.0 μm of sputtered silicon were compared to those from a commercial 7 μm poly(dimethylsiloxane) (PDMS) fiber. For mixtures of alcohols, aldehydes, amines, and esters, the 2.0 μm sputtered silicon fiber yielded signals that were 3-9, 3-5, 2.5-4.5, and 1.5-2 times higher, respectively, than those of the commercial fiber. For the heavier alkanes (undecane-hexadecane), the 2.0 μm sputtered fiber yielded signals that were approximately 1.0-1.5 times higher than the commercial fiber. The sputtered fibers extracted low molecular weight analytes that were not detectable with the commercial fiber. The selectivity of the sputtered fibers appears to favor analytes that have both a hydrophobic component and hydrogen-bonding capabilities. No detectable carryover between runs was noted for the sputtered fibers. The repeatability (RSD%) for a fiber (n = 3) was less than 10% for all analytes tested

  3. Nanocomposites obtained by embedding of conjugated polymers in porous silicon and silica

    NASA Astrophysics Data System (ADS)

    Errien, N.; Vellutini, L.; Froyer, G.; Louarn, G.; Simos, C.; Skarka, V.; Haesaert, S.; Joubert, P.

    2005-06-01

    Porous silicon and porous silica matrices are filled up by conjugated polymers in order to obtain nanocomposite with enhanced third order optical nonlinearity. The active component is either PDA-TS thermally polymerized in situ or PT12 electropolymerized in porous silicon. The first measurements of the nonlinear properties of these nanocomposites give evidence of a significant increase of the nonlinear refractive index with respect to the standard optical materials.

  4. Phosphonium salt incorporated hypercrosslinked porous polymers for CO2 capture and conversion.

    PubMed

    Wang, Jinquan; Wei Yang, Jason Gan; Yi, Guangshun; Zhang, Yugen

    2015-11-01

    Various novel hypercrosslinked porous polymers with phosphonium salt incorporated into their networks were developed. These porous materials have high BET surface areas (up to 1168 m(2) g(-1)) and can be used to selectively capture CO2 and efficiently convert CO2 into cyclic carbonates. PMID:26365361

  5. Microstructure and Properties of Porous Abradable Alumina Coatings Flame-Sprayed with Semi-molten Particles

    NASA Astrophysics Data System (ADS)

    Li, Chang-Jiu; Zou, Jiao; Huo, Hui-Bin; Yao, Jian-Tao; Yang, Guan-Jun

    2016-01-01

    High-efficiency gas turbines require high-temperature sealing by use of abradable porous ceramic coatings to increase engine efficiency. In this study, porous Al2O3 coatings were deposited by flame spraying; the coatings were applied in a semi-molten state by controlled melting of the sprayed powder particles. The effects of the degree of melting of the sprayed particles, which depends on spraying conditions, on coating microstructure and porosity were investigated. The degree of melting of the sprayed particles was characterized by use of 3D confocal laser microscopy. The porosity of the coating was estimated by image analysis. The results showed that the degree of melting of alumina particles can be changed from 70 to 30%, and thus coating porosity can be increased from 30% up to over 70%. The standard hardness test yielded no useful data for porous coatings deposited by use of sprayed particles with a degree of melting <60%, and a hardness of 32-75 HR15Y for Al2O3 coatings deposited by use of sprayed particles with a degree of melting >60%. Pin-on-disk abrasion tests, performed at room temperature by use of an Inconel 738 (IN738) nickel-based superalloy pin with a spherical tip 5 mm in diameter, were conducted on the porous alumina coating to evaluate its abrasion behavior. It was found that for coatings of hardness <32 HR15Y and porosity >40% the wear weight loss of the IN738 pin was negligible despite the high rate of wear of the coating. It is evident that flame-sprayed porous alumina coatings of high porosity prepared by this approach have potential for use as abradable coatings for gas turbines operating at high temperatures.

  6. Polymer derived ceramic composites as environmental barrier coatings on steel

    NASA Astrophysics Data System (ADS)

    Torrey, Jessica D.

    Polymer derived ceramics have shown promise as a novel way to process low-dimensional ceramics such as fibers and coatings. They offer advantages over traditional ceramic processing routes including lower pyrolysis temperatures and the ability to employ polymeric processing techniques. The main drawback to preceramic polymers is that they undergo a shrinkage during pyrolysis that can be greater than 50-volume%. One way to overcome this shrinkage is to add filler particles, usually elemental or binary metals, which will expand upon reaction with the pyrolysis atmosphere, thereby compensating for the shrinkage of the polymer. The aim of this study is to develop a polymer derived ceramic composite coating on steel as a barrier to oxidation and carburization, while concurrently gaining insight as to the fundamental mechanisms for compositional and microstructural evolution within the system. A systematic approach to selecting the preceramic polymer and expansion agents was taken. Six commercially available poly(silsesquioxane) polymers and a polysiloxane were studied. Several metals and an intermetallic were considered as potential expansion agents. The most desirable polymer/expansion agent combination was achieved with poly(hydridomethylsiloxane) as the matrix and titanium disilicide as the filler. Processing parameters have been optimized and a relationship derived to predict final coating thickness based on slurry viscosity and dip coating withdrawal speed. Microstructural analysis reveals an amorphous composite coating of oxidized filler particles in a silica matrix. A diffusion layer is visible at the coating-steel interface, indicating good bonding. The optimized coatings are ˜18mum thick, have some residual porosity and a density of 2.57g/cm3. A systematic study of the phase transformations and microstructural changes in the coating and its components during pyrolysis in air is also presented. The system evolves from a polymer filled with a binary metal at

  7. Photocatalytic TiO2 nanoparticles enhanced polymer antimicrobial coating

    NASA Astrophysics Data System (ADS)

    Wei, Xiaojin; Yang, Zhendi; Tay, See Leng; Gao, Wei

    2014-01-01

    Copper (Cu) containing coatings can provide sustainable protection against microbial contamination. However, metallic Cu coatings have not been widely used due to the relatively high cost, poor corrosion resistance, and low compatibility with non-metal substrates. Titanium dioxide (TiO2) possesses antibacterial functions by its photocatalytic properties which can destroy bacteria or suppress their reproduction. TiO2 also has the function of improving the mechanical properties through particle dispersion strengthening. We have recently developed an innovative polymer based coating system containing fine particles of Cu and TiO2 nanoparticles. These polymer based coatings simultaneously display excellent antimicrobial and good mechanical properties. The results showed that the addition of TiO2 has improved the antimicrobial property under sunlight, which provides extended applications in outdoor environment. The elimination of 106 bacterial by contacting the coatings without TiO2 needs 5 h, while contacting with the Cu/TiO2- 1 wt.% TiO2 took only 2 h to kill the same amount of bacteria. The coatings also presented enhanced hardness and wear resistance after adding TiO2. The width of wear track decreased from 270 μm of the Cu-polymer coating to 206 μm of Cu/TiO2-polymer coatings with 10 wt.% TiO2. Synchrotron Infrared Microscopy was used to in-situ and in-vivo study the bacteria killing process at the molecular level. The real-time chemical images of bacterial activities showed that the bacterial cell membranes were damaged by the Cu and TiO2 containing coatings

  8. Corrosion resistant coatings from conducting polymers

    SciTech Connect

    Wrobleski, D.A.; Benicewicz, B.C.; Thompson, K.G.; Bryan, C.J.

    1993-12-01

    Cr-based corrosion resistant undercoatings will have to be replaced because of environmental and health concerns. A coating system of a conducting polyaniline primer layer topcoated with epoxy or polyurethane, is being evaluated for corrosion resistance on mild steel in 0.1 M HCl or in a marine setting. Results of both laboratory and Beach Site testing indicate that this coating is very effective; even when the coatings are scratched to expose bare metal, the coated samples show very little signs of corrosion in the exposed area. 3 figs, 6 refs.

  9. Synthesis design of polar polymers and nanostructured porous silica

    NASA Astrophysics Data System (ADS)

    Schmidt-Winkel, Patrick Niels

    Nanostructured and functional materials have attracted a great deal of attention because of their importance for scientific and technological progress in our society. We have proposed a novel concept for functional, polar organic polymers that is based on the ferrielectric ordering of electric dipoles along the polymer backbone. In this context, a polar odd-numbered aliphatic polysulfone and low-molecular weight model compounds possessing remarkable thermal stability, degrading at 100°C above previously prepared polysulfones, have been synthesized and characterized. Mesoporous molecular sieves with uniform pores ranging from 2--50 nm in size are promising materials for catalysis, host-guest chemistry, separation, immobilization, encapsulation, insulation, etc. We have described a novel synthesis method to produce hierarchically ordered mesoporous silica in which the ordering on meso- to macroscopic length scales is controlled and significantly improved in one step. In search of a simple, efficient procedure to synthesize porous materials with ultralarge mesopores (30--50 nm), we have discovered microemulsions as novel colloidal templates for mesostructured cellular foams (MCFs). MCFs represent a new class of materials with well-defined, adjustable, and continuous ultralarge mesopores (9--42 nm). The microemulsion templating route has opened up new possibilities to engineer mesoporous systems for applications such as catalyst supports where mass transport is often limited by narrow pore openings. The microemulsion templates used to prepare MCF materials have been characterized by small-angle neutron scattering (SANS) studies. The microemulsion droplet size increases linearly with the cube root of the oil concentration, ethanol is required as cosurfactant, and the temperature behavior of the microemulsions is similar to the pure surfactant solution. In situ SANS studies of acid-synthesized SBA-15- and MCF-type silica have shown that silica condensation is fast early

  10. Synthesis of a further improved porous polymer for the separation of nitrogen, oxygen, argon, and carbon monoxide by gas chromatography

    NASA Technical Reports Server (NTRS)

    Pollock, G. E.

    1986-01-01

    A further improvement has been made in the synthesis of an N-type porous polymer for the separation of permanent gases. Changing the ratios of reactants and diluting the Hi-DVB with styrene led to a porous polymer gas chromatographic packing which is superior to commercial products and to the author's own previously reported custom-made polymer.

  11. Ordered mesoporous polymers in situ coated on a stainless steel wire for a highly sensitive solid phase microextraction fibre

    NASA Astrophysics Data System (ADS)

    Zheng, Juan; Liang, Yeru; Liu, Shuqin; Ding, Yajuan; Shen, Yong; Luan, Tiangang; Zhu, Fang; Jiang, Ruifen; Wu, Dingcai; Ouyang, Gangfeng

    2015-07-01

    Development of facile and effective methods for fabrication of high-performance solid phase microextraction (SPME) fibres remains a great challenge. Herein, a new class of ordered mesoporous polymers (OMPs) in situ coated on a stainless steel wire were successfully developed and utilized as a highly sensitive and stable SPME fibre for the first time. Because of the highly ordered mesoporous structure of its OMP coating, the π-π interactions and the dispersion forces, the OMP-coated SPME fibre exhibited much better extraction properties as compared to the commercial PDMS fibre. The findings could provide a new benchmark for preparing well-defined porous materials for the SPME application.Development of facile and effective methods for fabrication of high-performance solid phase microextraction (SPME) fibres remains a great challenge. Herein, a new class of ordered mesoporous polymers (OMPs) in situ coated on a stainless steel wire were successfully developed and utilized as a highly sensitive and stable SPME fibre for the first time. Because of the highly ordered mesoporous structure of its OMP coating, the π-π interactions and the dispersion forces, the OMP-coated SPME fibre exhibited much better extraction properties as compared to the commercial PDMS fibre. The findings could provide a new benchmark for preparing well-defined porous materials for the SPME application. Electronic supplementary information (ESI) available: Experimental details, Fig. S1-S3 and Tables S1-S3. See DOI: 10.1039/c5nr02674a

  12. Computational Strategies for Polymer Coated Steel Sheet Forming Simulations

    SciTech Connect

    Owen, D. R. J.; Andrade Pires, F. M.; Dutko, M.

    2007-05-17

    This contribution discusses current issues involved in the numerical simulation of large scale industrial forming processes that employ polymer coated steel sheet. The need for rigorous consideration of both theoretical and algorithmic issues is emphasized, particularly in relation to the computational treatment of finite strain deformation of polymer coated steel sheet in the presence of internal degradation. Other issues relevant to the effective treatment of the problem, including the modelling of frictional contact between the work piece and tools, low order element technology capable of dealing with plastic incompressibility and thermo mechanical coupling, are also addressed. The suitability of the overall approach is illustrated by the solution of an industrially relevant problem.

  13. Hydrophobic and oleophobic coating technologies for polymer optics

    NASA Astrophysics Data System (ADS)

    Fiore, Daniel; Wilson, Brian

    2012-10-01

    With the array of thin-film coated polymer based optics currently in use within the optoelectronic and photonic industries the need for finger print reducing coatings has drastically increased. Due to the peak-to-valley micro structure of thinfilms fingerprint oils and other airborne particulate are prone to create disruptive optical interference within films, which negate their overall effectiveness in transmitting light and or data. Our approach in combating this issue is a deposition process that is capable of being deposited on numerous injection-molded and cast sheet polymer formulations to help reduce the appearance of fingerprint oils on optically and cosmetically critical components. In many cases, such vacuum-applied coatings improve the optical performance of polymers by improving the visual acuity of the display through the drastic reduction of fingerprint oils and airborne particulate. This presentation will focus on the full spectrum of thin-film coatings that are currently being deployed to polymer optics in order to combat smudging and fingerprints on polymer optics and displays.

  14. Antifungal activity of polymer-based copper nanocomposite coatings

    NASA Astrophysics Data System (ADS)

    Cioffi, Nicola; Torsi, Luisa; Ditaranto, Nicoletta; Sabbatini, Luigia; Zambonin, Pier Giorgio; Tantillo, Giuseppina; Ghibelli, Lina; D'Alessio, Maria; Bleve-Zacheo, Teresa; Traversa, Enrico

    2004-09-01

    Eukaryotes, such as fungi, can be harmful pathogen agents, and the control of their bioactivity is critical as humans are eukaryote organisms, too. Here, copper/polymer nanocomposites are proposed as antifungal spinnable coatings with controlled copper-releasing properties. The tests of the bioactivity show that fungal growth is inhibited on the nanocomposite-coated plates, and the antifungal activity can be modulated by controlling the Cu nanoparticle loading.

  15. Surface-initiated hyperbranched polyglycerol as an ultralow-fouling coating on glass, silicon, and porous silicon substrates.

    PubMed

    Moore, Eli; Delalat, Bahman; Vasani, Roshan; McPhee, Gordon; Thissen, Helmut; Voelcker, Nicolas H

    2014-09-10

    Anionic ring-opening polymerization of glycidol was initiated from activated glass, silicon, and porous silicon substrates to yield thin, ultralow-fouling hyperbranched polyglycerol (HPG) graft polymer coatings. Substrates were activated by deprotonation of surface-bound silanol functionalities. HPG polymerization was initiated upon the addition of freshly distilled glycidol to yield films in the nanometer thickness range. X-ray photoelectron spectroscopy, contact angle measurements, and ellipsometry were used to characterize the resulting coatings. The antifouling properties of HPG-coated surfaces were evaluated in terms of protein adsorption and the attachment of mammalian cells. The adsorption of bovine serum albumin and collagen type I was found to be reduced by as much as 97 and 91%, respectively, in comparison to untreated surfaces. Human glioblastoma and mouse fibroblast attachment was reduced by 99 and 98%, respectively. HPG-grafted substrates outperformed polyethylene glycol (PEG) grafted substrates of comparable thickness under the same incubation conditions. Our results demonstrate the effectiveness of antifouling HPG graft polymer coatings on a selected range of substrate materials and open the door for their use in biomedical applications. PMID:25137525

  16. In vitro and in vivo characterization of porous poly-l-lactic acid coatings for subcutaneously implanted glucose sensors

    PubMed Central

    Koschwanez, H. E.; Yap, F. Y.; Klitzman, B.; Reichert, W. M.

    2014-01-01

    The purpose of this study was to test the hypothesis that porous poly-l-lactic acid (PLLA) sensor coatings reduce fibrosis and promote blood microvessel formation in tissue adjacent to the sensor surface. Porous PLLA coatings were produced using ammonium bicarbonate as the gas foaming/salt leaching agent, and deployed on functional and nonfunctional sensors. The porous coatings minimally affected sensor accuracy and response rate in vitro. Three-week subcutaneous rat studies of nonfunctional glucose sensors showed the anticipated effect of porous coatings enhancing vascularity and decreasing collagen deposition. In contrast, percutaneous functional sensors with and without porous coatings showed no significant difference in terms of histology or sensor response. In spite of the observation that texturing increases the vascularity of the tissue that surrounds implanted sensors, other factors such as the additional mechanical stresses imposed by percutaneous tethering may override the beneficial effects of the porous coatings. PMID:18200540

  17. Polyaniline: a conductive polymer coating for durable nanospray emitters

    PubMed

    Maziarz; Lorenz; White; Wood

    2000-07-01

    Despite the tremendous sensitivity and lower sample requirements for nanospray vs. conventional electrospray, metallized nanospray emitters have suffered from one of two problems: low mechanical stability (leading to emitter failure) or lengthy, tedious production methods. Here, we describe a simple alternative to metallized tips using polyaniline (PANI), a synthetic polymer well known for its high conductivity, anticorrosion properties, antistatic properties, and mechanical stability. A simple method for coating borosilicate emitters (1.2 mm o.d.) pulled to fine tapers (4 +/- 1 microm) with water-soluble and xylene-soluble dispersions of conductive polyaniline (which allows for electrical contact at the emitter outlet) is described. The polyaniline-coated emitters show high durability and are resistant to electrical discharge, likely because of the thick (yet optically transparent) coatings; a single emitter can be used over a period of days for multiple samples with no visible indication of the destruction of the polyaniline coating. The optical transparency of the coating also allows the user to visualize the sample plug loaded into the emitter. Examples of nanospray using coatings of the water-soluble and xylene-soluble polyaniline dispersions are given. A comparison of PANI-coated and gold-coated nanospray emitters to conventional electrospray ionization (ESI) show that PANI-coated emitters provide similar enhanced sensitivity that gold-coated emitters exhibit vs. conventional ESI. PMID:10883822

  18. Porous devices derived from co-continuous polymer blends as a route for controlled drug release.

    PubMed

    Salehi, Pouneh; Sarazin, Pierre; Favis, Basil D

    2008-04-01

    In this study we examine the release profile of bovine serum albumin (BSA) from a porous polymer matrix derived from a co-continuous polymer blend. The porosity is generated through the selective extraction of one of the continuous phases. This is the first study to examine the approach of using morphologically tailored co-continuous polymer blends as a template for generating porous polymer materials for use in controlled release. A method for the preparation of polymeric capsules is introduced, and the effect of matrix pore size and surface area on the BSA release profile is investigated. Furthermore, the effect of surface charge on release is examined by surface modification of the porous substrate using layer-by-layer deposition techniques. Synthetic, nonerodible polymer, high-density polyethylene (HDPE), was used as a model substrate prepared by melt blending with two different styrene-ethylene-butylene copolymers. Blends with HDPE allow for the preparation of porous substrates with small pore sizes (300 and 600 nm). A blend of polylactide (PLA) and polystyrene was also used to prepare porous PLA with a larger pore size (1.5 microm). The extents of interconnectivity, surface area, and pore dimension of the prepared porous substrates were examined via gravimetric solvent extraction, BET nitrogen adsorption, mercury porosimetry, and image analysis of scanning electron microscopy micrographs. With a loading protocol into the porous HDPE and PLA involving the alternate application of pressure and vacuum, it is shown that virtually the entire porous network was accessible to BSA loading, and loading efficiencies of between 80% and 96% were obtained depending on the pore size of the carrier and the applied pressure. The release profile of BSA from the microporous structure was monitored by UV spectrophotometry. The influence of pore size, surface area, surface charge, and number of deposited layers is demonstrated. It is shown that an effective closed-cell structure

  19. Development and characterization of porous polypyrrole-polylactic acid electroactive polymer blends

    NASA Astrophysics Data System (ADS)

    Chan, Christine; Chan, Ellen; Naguib, Hani E.

    2009-03-01

    Conducting polymers have sparked much research interest due to their unique ability to be electrically stimulated. However, these polymers are very brittle and have poor mechanical properties. In order to improve upon its structural integrity, it can be blended with other host polymers that have better mechanical properties. These blended composites would then possess the benefits of conductive properties while having sufficient mechanical properties to be more suitable for practical applications. Polypyrrole-polylactic acid blends were processed using chemical oxidative polymerization and compression molding, followed by gas foaming and saturation techniques to create porous structures. Characterization of these porous blends included its physical, thermal, and mechanical properties.

  20. Design of nanocomposite polymer coatings for MEMS applications

    NASA Astrophysics Data System (ADS)

    Julthongpiput, Duangrut

    The recent evolution in microelectronics of combining electrical and mechanical functions has brought about the exciting field of microelectromechanical system (MEMS). As the dimensions of the components shrink, adhesion, stiction, friction, and wear become a significant technological barrier for the successful development of durable microdevices. In this thesis, we investigate wear-resistant, nanocomposite, molecular coatings from advanced polymers with controlled nanomechanical and nanotribological properties from the prospective of long-term applications for MEMS. We discuss fundamentals governing the mechanical and tribological properties on a micro scale associated with the morphology and microstructure of these molecular coatings. In order to fabricate wear-resistant and superelastic molecular coatings, several types of the molecular designs are proposed and tested in this work. All designs are based on chemical attachment of the polymer layers onto a functionalized silicon surface. We focus on developing two different kinds of molecular coatings: reinforced elastomeric layers from grafted block-copolymers and polymer brush layers grown by the "grafted to" technique. A more complicated design included bilayered nanocomposite coatings consisting of a hard polymer layer placed on the top of an elastomeric layer to regulate surface adhesion and to increase surface stiffness of nanocomposite bilayers. Another design incorporates a paraffinic oil component to assure the presence of highly mobile molecules inside of the elastomeric phase. This oily fraction can be a source of an instant supply of mobile lubricant to a deformed contact area, thus providing potential self-lubrication and self-healing mechanisms for surface areas affected by excessive deformation. We observed that the interfacial assemblies, as presented in this paper, exhibited very low friction coefficient, low stiction, and better wear stability as compared to other, non-structured, non

  1. Protective coatings for high-temperature polymer matrix composites

    NASA Technical Reports Server (NTRS)

    Harding, David R.; Sutter, James K.; Papadopoulos, Demetrios S.

    1993-01-01

    Plasma-enhanced chemical vapor deposition was used to deposit silicon nitride on graphite-fiber-reinforced polyimide composites to protect against oxidation at elevated temperatures. The adhesion and integrity of the coating were evaluated by isothermal aging (371 C for 500 hr) and thermal cycling. The amorphous silicon nitride (a-SiN:H) coating could withstand stresses ranging from approximately 0.18 GPa (tensile) to -1.6 GPa (compressive) and provided a 30 to 80 percent reduction in oxidation-induced weight loss. The major factor influencing the effectiveness of a-SiN:H as a barrier coating against oxidation is the surface finish of the polymer composite.

  2. The shear strength of three-dimensional capillary-porous titanium coatings for intraosseous implants.

    PubMed

    Kalita, V I; Komlev, D I; Komlev, V S; Radyuk, A A

    2016-03-01

    A plasma spraying process for the deposition of three-dimensional capillary-porous titanium coatings using a wire has been developed. In this process, two additional dc arcs are discharged between plasmatron and both the wire and the substrate, resulting in additional activation of the substrate and the particles, particularly by increasing their temperature. The shear strength of the titanium coating with 46% porosity is 120.6 MPa. A new procedure for estimating the shear strength of porous coatings has been developed. PMID:26706529

  3. Protection of moisture-sensitive drugs with aqueous polymer coatings: importance of coating and curing conditions.

    PubMed

    Bley, O; Siepmann, J; Bodmeier, R

    2009-08-13

    The aim of this study was to better understand the importance of coating and curing conditions of moisture-protective polymer coatings. Tablets containing freeze-dried garlic powder were coated with aqueous solutions/dispersions of hydroxypropyl methylcellulose (HPMC), poly(vinyl alcohol), ethyl cellulose and poly(methacrylate-methylmethacrylates). The water content of the tablets during coating and during storage at different temperatures and relative humidities (RH) was determined gravimetrically. In addition, changes in the allicin (active ingredient in garlic powder) content were monitored. During the coating process, the water uptake was below 2.7% and no drug degradation was detectable. Thermally induced drug degradation occurred only at temperatures above the coating temperatures. Different polymer coatings effectively decreased the rate, but not the extent of water uptake during open storage at room temperature and 75% RH. Tablets coated with poly(vinyl alcohol) and poly(methacrylate-methylmethacrylates) showed the lowest moisture uptake rates (0.49 and 0.57%/d, respectively). Curing at elevated temperature after coating did not improve the moisture-protective ability of the polymeric films, but reduced the water content of the tablets. Drug stability was significantly improved with tablets coated with poly(vinyl alcohol) and poly(methacrylate-methylmethacrylates). PMID:19477253

  4. Mössbauer Investigation of Highly Dispersed Iron Particles in Crazed Porous Polymers

    NASA Astrophysics Data System (ADS)

    Trofimchuk, E. S.; Nikonorova, N. I.; Dedushenko, S. K.; Perfiliev, Y. D.

    2004-12-01

    Formation and stability of highly dispersed iron particles in crazed porous polymer matrices were studied. The iron polymer composites obtained were characterized by different morphologies and dimensions of iron particles. The phase content of the iron constituent in a composite studied by Mössbauer spectroscopy was shown to depend on the type of the iron salt and the method of introduction of the initial reagents into a polymer.

  5. Estimating attachment of nano- and submicrometer-particles coated with organic macromolecules in porous media: development of an empirical model.

    PubMed

    Phenrat, Tanapon; Song, Jee Eun; Cisneros, Charlotte M; Schoenfelder, Daniel P; Tilton, Robert D; Lowry, Gregory V

    2010-06-15

    Assessing the environmental transport and fate of manufactured nanoparticles (NPs) and potential exposure risks requires models for predicting attachment of NPs coated with organic macromolecules in porous media. The objective of this study was to determine the properties of coated nanoparticles that control their attachment behavior. Deposition data for a variety of nanoparticles with different types of anionic organic coatings, including natural organic matter (NOM)-coated latex and hematite nanoparticles, and poly(styrenesulfonate)-, carboxymethylcellulose-, and polyaspartate-coated hematite and titanium dioxide nanoparticles (80 data points), were used to develop an empirical correlation between measurable NP properties and their sticking coefficient (alpha) under a variety of electrolyte conditions and flow velocities. Available semiempirical correlations used to predict the attachment efficiency of electrostatically stabilized (uncoated) NPs overestimate the attachment efficiency of nanoparticles coated with NOM or synthetic polyelectrolytes because the correlations neglect electrosteric repulsions and the decreased friction afforded by such coatings that can inhibit attachment to surfaces. Adding a dimensionless parameter (N(LEK)) representing steric repulsions and the decreased friction force afforded by adsorbed NOM or anionic polyelectrolytes in the correlation significantly improves the correlation. This establishes the importance of including the adsorbed NOM- or polyelectrolyte layer properties for estimating the attachment efficiency of NPs in the environment. The form of N(LEK) suggests that limiting unintended transport and exposure to NPs could be achieved by using coatings with the smallest adsorbed mass and polymer density, shortest extended layer thickness, and largest molecular weight that would still afford the desired functionality of the coating. PMID:20465214

  6. Long-lasting Antifouling Coating from Multi-Armed Polymer

    PubMed Central

    Mizrahi, Boaz; Khoo, Xiaojuan; Chaing, Homer H.; Sher, Katalina J.; Feldman, Rose G.; Lee, Jung-Jae; Irusta, Silvia; Kohane, Daniel S.

    2013-01-01

    We describe a new antifouling surface coating, based on aggregation of a short amphiphilic four-armed PEG-dopamine polymer into particles, and on surface binding by catechol chemistry. An unbroken and smooth polymeric coating layer with an average thickness of approximately 4 microns was formed on top of titanium oxide surfaces by a single step reaction. Coatings conferred excellent resistance to protein adhesion. Cell attachment was completely prevented for at least eight weeks, although the membranes themselves did not appear to be intrinsically cytotoxic. When linear PEG or four-armed PEG of higher molecular weight were used, the resulting coatings were inferior in thickness and in preventing protein adhesion. This coating method has potential applicability for biomedical devices susceptible to fouling after implantation. PMID:23855875

  7. Metallated porphyrin based porous organic polymers as efficient electrocatalysts

    NASA Astrophysics Data System (ADS)

    Lu, Guolong; Zhu, Youlong; Xu, Kongliang; Jin, Yinghua; Ren, Zhiyong Jason; Liu, Zhenning; Zhang, Wei

    2015-10-01

    Developing efficient, stable and low-cost catalysts for Oxygen Reduction Reaction (ORR) is of great significance to many emerging technologies including fuel cells and metal-air batteries. Herein, we report the development of a cobalt(ii) porphyrin based porous organic polymer (CoPOP) and its pyrolyzed derivatives as highly active ORR catalysts. The as-synthesized CoPOP exhibits high porosity and excellent catalytic performance stability, retaining ~100% constant ORR current over 50 000 s in both alkaline and acidic media. Pyrolysis of CoPOP at various temperatures (600 °C, 800 °C, and 1000 °C) yields the materials consisting of graphitic carbon layers and cobalt nanoparticles, which show greatly enhanced catalytic activity compared to the as-synthesized CoPOP. Among them, CoPOP-800/C pyrolyzed at 800 °C shows the highest specific surface area and ORR activity, displaying the most positive half-wave potential (0.825 V vs. RHE) and the largest limited diffusion current density (5.35 mA cm-2) in an alkaline medium, which are comparable to those of commercial Pt/C (20 wt%) (half-wave potential 0.829 V vs. RHE, limited diffusion current density 5.10 mA cm-2). RDE and RRDE experiments indicate that CoPOP-800/C directly reduces molecular oxygen to water through a 4-e- pathway in both alkaline and acidic media. More importantly, CoPOP-800/C exhibits excellent durability and methanol-tolerance under acidic and alkaline conditions, which surpass the Pt/C (20 wt%) system.Developing efficient, stable and low-cost catalysts for Oxygen Reduction Reaction (ORR) is of great significance to many emerging technologies including fuel cells and metal-air batteries. Herein, we report the development of a cobalt(ii) porphyrin based porous organic polymer (CoPOP) and its pyrolyzed derivatives as highly active ORR catalysts. The as-synthesized CoPOP exhibits high porosity and excellent catalytic performance stability, retaining ~100% constant ORR current over 50 000 s in both

  8. Simultaneous sorption and mechanical entrapment during polymer flow through porous media

    NASA Astrophysics Data System (ADS)

    Farajzadeh, R.; Bedrikovetsky, P.; Lotfollahi, M.; Lake, L. W.

    2016-03-01

    Physical adsorption and mechanical entrapment are two major causes of polymer retention in porous media. Physical adsorption is considered an equilibrium process and is often modeled by assuming a Langmuir isotherm. The outcome is a steady state pressure response because the permeability reduction is also accounted for by adsorption. However, some experimental data show gradual increase of pressure with time, implying that polymer retention is a time-dependent process. We discuss simultaneous effect of sorption and mechanical entrapment on the polymer retention in porous media. An exact solution for 1-D flow problem for the case of constant filtration coefficient and Langmuir-sorption isotherm, including explicit formulae for breakthrough concentration and pressure drop across the core is derived. The general model with a varying filtration coefficient was successfully matched with experimental data confirming the occurrence of simultaneous sorption with deep-bed filtration during polymer flow in porous media. In the absence of mechanical entrapment, the physical adsorption causes delay in the polymer front and does not affect the polymer concentration behind the front. Addition of mechanical entrapment results in slow recovery of the injected concentration at the outlet (for a varying filtration coefficient) or reaching to a steady state concentration, which is only a fraction of the injected concentration (for a constant filtration coefficient). Accurate assessment and quantification of the polymer retention requires both pressure and effluent concentration data at the outlet of the porous medium.

  9. Metallated porphyrin based porous organic polymers as efficient electrocatalysts.

    PubMed

    Lu, Guolong; Zhu, Youlong; Xu, Kongliang; Jin, Yinghua; Ren, Zhiyong Jason; Liu, Zhenning; Zhang, Wei

    2015-11-21

    Developing efficient, stable and low-cost catalysts for Oxygen Reduction Reaction (ORR) is of great significance to many emerging technologies including fuel cells and metal-air batteries. Herein, we report the development of a cobalt(II) porphyrin based porous organic polymer (CoPOP) and its pyrolyzed derivatives as highly active ORR catalysts. The as-synthesized CoPOP exhibits high porosity and excellent catalytic performance stability, retaining ∼100% constant ORR current over 50,000 s in both alkaline and acidic media. Pyrolysis of CoPOP at various temperatures (600 °C, 800 °C, and 1000 °C) yields the materials consisting of graphitic carbon layers and cobalt nanoparticles, which show greatly enhanced catalytic activity compared to the as-synthesized CoPOP. Among them, CoPOP-800/C pyrolyzed at 800 °C shows the highest specific surface area and ORR activity, displaying the most positive half-wave potential (0.825 V vs. RHE) and the largest limited diffusion current density (5.35 mA cm(-2)) in an alkaline medium, which are comparable to those of commercial Pt/C (20 wt%) (half-wave potential 0.829 V vs. RHE, limited diffusion current density 5.10 mA cm(-2)). RDE and RRDE experiments indicate that CoPOP-800/C directly reduces molecular oxygen to water through a 4-e(-) pathway in both alkaline and acidic media. More importantly, CoPOP-800/C exhibits excellent durability and methanol-tolerance under acidic and alkaline conditions, which surpass the Pt/C (20 wt%) system. PMID:26486413

  10. Reptation of a semiflexible polymer through porous media

    NASA Astrophysics Data System (ADS)

    Nam, Gimoon; Johner, Albert; Lee, Nam-Kyung

    2010-07-01

    We study the motion of a single stiff semiflexible filament of length S through an array of topological obstacles. By means of scaling arguments and two-dimensional computer simulations, we show that the stiff chain kinetics follows the reptation picture, albeit with kinetic exponents (for the central monomer) different from those for flexible chain reptation. At early times when topological constraints are irrelevant, the chain kinetics is the anisotropic dynamics of a free filament. After the entanglement time τe transverse modes are equilibrated under the topological constraints, but the chain is not yet correlated over its whole length. During the relaxation of longitudinal modes, both the longitudinal fluctuation of the central monomer and the longitudinal correlation length grow as ˜√t . After time τr˜S2 chain ends are correlated, the chain then diffuses globally along the tube and tube renewal takes place. In the reptation regime, the longitudinal fluctuation of the central monomer grows like ˜t1. The opening of the intermediate ˜√t regime, absent for a free filament, is a signature of the reptation process. Although the underlying physics is quite different, the intermediate regime is reminiscent of the internal Rouse mode relaxation found for reptating flexible chains. In most cases asymptotic power laws from scaling could be complemented by prefactors calculated analytically. Our results are supported by two-dimensional Langevin simulations with fixed obstacles via evaluation of the mean squared displacement of the central monomer. The scaling theory can be extended to long semiflexible polymers adopting random-walk equilibrium configurations and should also apply in three dimensions for porous media with pore diameter smaller than the persistence length of the filament.

  11. Thermal Protective Coating for High Temperature Polymer Composites

    NASA Technical Reports Server (NTRS)

    Barron, Andrew R.

    1999-01-01

    The central theme of this research is the application of carboxylate-alumoxane nanoparticles as precursors to thermally protective coatings for high temperature polymer composites. In addition, we will investigate the application of carboxylate-alumoxane nanoparticle as a component to polymer composites. The objective of this research was the high temperature protection of polymer composites via novel chemistry. The significance of this research is the development of a low cost and highly flexible synthetic methodology, with a compatible processing technique, for the fabrication of high temperature polymer composites. We proposed to accomplish this broad goal through the use of a class of ceramic precursor material, alumoxanes. Alumoxanes are nano-particles with a boehmite-like structure and an organic periphery. The technical goals of this program are to prepare and evaluate water soluble carboxylate-alumoxane for the preparation of ceramic coatings on polymer substrates. Our proposed approach is attractive since proof of concept has been demonstrated under the NRA 96-LeRC-1 Technology for Advanced High Temperature Gas Turbine Engines, HITEMP Program. For example, carbon and Kevlar(tm) fibers and matting have been successfully coated with ceramic thermally protective layers.

  12. Porous niobium coatings fabricated with selective laser melting on titanium substrates: Preparation, characterization, and cell behavior.

    PubMed

    Zhang, Sheng; Cheng, Xian; Yao, Yao; Wei, Yehui; Han, Changjun; Shi, Yusheng; Wei, Qingsong; Zhang, Zhen

    2015-08-01

    Nb, an expensive and refractory element with good wear resistance and biocompatibility, is gaining more attention as a new metallic biomaterial. However, the high price of the raw material, as well as the high manufacturing costs because of Nb's strong oxygen affinity and high melting point have limited the widespread use of Nb and its compounds. To overcome these disadvantages, porous Nb coatings of various thicknesses were fabricated on Ti substrate via selective laser melting (SLM), which is a 3D printing technique that uses computer-controlled high-power laser to melt the metal. The morphology and microstructure of the porous Nb coatings, which had pores ranging from 15 to 50 μm in size, were characterized with scanning electron microscopy (SEM). The average hardness of the coating, which was measured with the linear intercept method, was 392±37 HV. In vitro tests of the porous Nb coating which was monitored with SEM, immunofluorescence, and CCK-8 counts of cells, exhibited excellent cell morphology, attachment, and growth. The simulated body fluid test also proved the bioactivity of the Nb coating. Therefore, these new porous Nb coatings could potentially be used for enhanced early biological fixation to bone tissue. In addition, this study has shown that SLM technique could be used to fabricate coatings with individually tailored shapes and/or porosities from group IVB and VB biomedical metals and their alloys on stainless steel, Co-Cr, and other traditional biomedical materials without wasting raw materials. PMID:26042690

  13. Osteointegration of biomimetic apatite coating applied onto dense and porous metal implants in femurs of goats.

    PubMed

    Barrère, F; van der Valk, C M; Meijer, G; Dalmeijer, R A J; de Groot, K; Layrolle, P

    2003-10-15

    Biomimetic calcium phosphate (Ca-P) coatings were applied onto dense titanium alloy (Ti6Al4V) and porous tantalum (Ta) cylinders by immersion into simulated body fluid at 37 degrees C and then at 50 degrees C for 24 h. As a result, a homogeneous bone-like carbonated apatitic (BCA) coating, 30 microm thick was deposited on the entire surface of the dense and porous implants. Noncoated and BCA-coated implants were press-fit implanted in the femoral diaphysis of 14 adult female goats. Bone contact was measured after implantation for 6, 12, and 24 weeks, and investigated by histology and backscattered electron microscopy (BSEM). After 6 weeks, bone contact of the BCA-coated Ti6Al4V implants was about 50%. After 12 and 24 weeks, bone contact was lower in comparison with the 6-week implantations at, respectively 24 and 39%. Regarding the BCA-coated porous Ta implants, bone contacts were 17, 30, and 18% after 6, 12, and 24 weeks, respectively. However, bone contact was always found significantly higher for BCA-coated dense Ti6Al4V and porous Ta cylinders than the corresponding noncoated implants. The results of this study show that the BCA coating enhances the bone integration as compared to the noncoated implants. PMID:14528464

  14. Biomimetic calcium phosphate coating of additively manufactured porous CoCr implants

    NASA Astrophysics Data System (ADS)

    Lindahl, Carl; Xia, Wei; Engqvist, Håkan; Snis, Anders; Lausmaa, Jukka; Palmquist, Anders

    2015-10-01

    The aim of this work was to study the feasibility to use a biomimetic method to prepare biomimetic hydroxyapatite (HA) coatings on CoCr substrates with short soaking times and to characterize the properties of such coatings. A second objective was to investigate if the coatings could be applied to porous CoCr implants manufactured by electron beam melting (EBM). The coating was prepared by immersing the pretreated CoCr substrates and EBM implants into the phosphate-buffered solution with Ca2+ in sealed plastic bottles, kept at 60 °C for 3 days. The formed coating was partially crystalline, slightly calcium deficient and composed of plate-like crystallites forming roundish flowers in the size range of 300-500 nm. Cross-section imaging showed a thickness of 300-500 nm. In addition, dissolution tests in Tris-HCl up to 28 days showed that a substantial amount of the coating had dissolved, however, undergoing only minor morphological changes. A uniform coating was formed within the porous network of the additive manufactured implants having similar thickness and morphology as for the flat samples. In conclusion, the present coating procedure allows coatings to be formed on CoCr and could be used for complex shaped, porous implants made by additive manufacturing.

  15. Simple fabrication of a three-dimensional porous polymer film as a diffuser for organic light emitting diodes

    NASA Astrophysics Data System (ADS)

    Lim, Byung Wan; Suh, Min Chul

    2014-11-01

    We have investigated a simple and cost-effective fabrication method for a porous polymer film employing the spin-coating process during continuous supply of water droplets by an ultrasonic humidifier. The resulting porous polymer film showed ~40% optical haze, and this film could be used as a diffuser film for strong microcavity OLEDs. Specifically, we focused on controlling the surface morphology to give a three-dimensional (3D) multi-stacked nanocave structure because we had already learnt that two-dimensional nanoporous structures showed serious loss of luminance in the forward direction. As a result, we found that a 3D-ordered multi-stacked nanocave structure with a relatively small diameter and a distribution range of 300-500 nm can be obtained by precise control of the elastic bouncing behaviour of the supplied water droplets. Using this approach, we found that the 3D nanoporous polymer film can effectively reduce the viewing angle dependency of strong microcavity OLEDs without any considerable decrease in the total intensity of the out-coupled light.

  16. Hierarchical polymer coating for optimizing the antifouling and bactericidal efficacies.

    PubMed

    Yan, Shunjie; Song, Lingjie; Li, Zhihong; Luan, Shifang; Shi, Hengchong; Xin, Zhirong; Li, Shenghai; Yang, Yuming; Yin, Jinghua

    2016-10-01

    The bacteria-repellent and bactericidal functionalities in a single system are generally need to be carefully optimized in order to obtain the highest antibacterial performance. In this study, the controlled SI-PIMP strategy was developed for creating hierarchical polymer brushes possessing the bacteria-repellent and bactericidal functionalities. To obtain a bactericidal surface with minimal interference to its nonfouling property, optimization studies were conducted by facilely tailoring the surface density of the quaternary ammonium compound moieties through control over the monomer concentration. An optimal hierarchical polymer coating showed potent protein and bacteria repellence as well as certain bactericidal property. The longlasting antibacterial performance was also achieved due to the good balance between the dual functionalities. The tenability of the hierarchical polymer coating is applicable to surface chemistries for biosensors, molecular imaging, and biomedical applications. PMID:27363527

  17. Mussel-inspired dendritic polymers as universal multifunctional coatings.

    PubMed

    Wei, Qiang; Achazi, Katharina; Liebe, Hendrik; Schulz, Andrea; Noeske, Paul-Ludwig Michael; Grunwald, Ingo; Haag, Rainer

    2014-10-20

    A rapid and universal approach for multifunctional material coatings was developed based on a mussel-inspired dendritic polymer. This new kind of polymer mimics not only the functional groups of mussel foot proteins (mfps) but also their molecular weight and molecular structure. The large number of catechol and amine groups set the basis for heteromultivalent anchoring and crosslinking. The molecular weight reaches 10 kDa, which is similar to the most adhesive mussel foot protein mfp-5. Also, the dendritic structure exposes its functional groups on the surface like the folded proteins. As a result, a very stable coating can be prepared on virtually any type of material surface within 10 min by a simple dip-coating method, which is as fast as the formation of mussel byssal threads in nature. PMID:25200129

  18. Biodegradable polymer brush as nanocoupled interface for improving the durability of polymer coating on metal surface.

    PubMed

    Bedair, Tarek M; Cho, Youngjin; Joung, Yoon Ki; Han, Dong Keun

    2014-10-01

    Metal-based drug-eluting stents (DESs) have severe drawbacks such as peeling-off and cracking of the coated polymer. To prevent the fracture of polymer-coated layer and improve the durability of DES, poly(l-lactide) (PLLA) brushes were synthesized onto cobalt-chromium (Co-Cr or CC) surface through atom transfer radical polymerization (ATRP) of 2-hydroxyethylmethacrylate (HEMA) followed by surface-initiated ring opening polymerization (SI-ROP) of l-lactide. The polymer brushes were then characterized by attenuated total reflection-Fourier transform infrared (ATR-FTIR), water contact angle, ellipsometry, X-ray photoelectron spectroscopy (XPS), atomic force microscopy (AFM), and scanning electron microscopy (SEM). All of the unmodified and modified Co-Cr surfaces were coated with a matrix of poly(d,l-lactide) (PDLLA) and sirolimus (SRL). The in vitro drug release profile was measured for 70 days. The PLLA-modified Co-Cr showed a biphasic release pattern in the initial burst followed by a slow release. On the other hand, the unmodified Co-Cr showed fast drug release and detachment of the coated polymer layer due to the instability of the polymer layer on Co-Cr surface. In comparison, the PLLA-modified Co-Cr preserved a uniform coating without detachment even after 6 weeks of degradation test. The platelet morphology and low density of platelet adhered on the modified layer and the SRL-in-PDLLA coated Co-Cr surfaces demonstrated that these samples would be blood compatible. Therefore, the introduction of PLLA brush onto Co-Cr surface is proved to dramatically improve the durability of the coating layer, and it is a promising strategy to prevent the coating defects found in DESs. PMID:25200098

  19. Pool boiling of nanofluids on rough and porous coated tubes: experimental and correlation

    NASA Astrophysics Data System (ADS)

    Cieśliński, Janusz T.; Kaczmarczyk, Tomasz Z.

    2014-06-01

    The paper deals with pool boiling of water-Al2O3 and water- Cu nanofluids on rough and porous coated horizontal tubes. Commercially available stainless steel tubes having 10 mm outside diameter and 0.6 mm wall thickness were used to fabricate the test heater. The tube surface was roughed with emery paper 360 or polished with abrasive compound. Aluminium porous coatings of 0.15 mm thick with porosity of about 40% were produced by plasma spraying. The experiments were conducted under different absolute operating pressures, i.e., 200, 100, and 10 kPa. Nanoparticles were tested at the concentration of 0.01, 0.1, and 1% by weight. Ultrasonic vibration was used in order to stabilize the dispersion of the nanoparticles. It was observed that independent of operating pressure and roughness of the stainless steel tubes addition of even small amount of nanoparticles augments heat transfer in comparison to boiling of distilled water. Contrary to rough tubes boiling heat transfer coefficient of tested nanofluids on porous coated tubes was lower compared to that for distilled water while boiling on porous coated tubes. A correlation equation for prediction of the average heat transfer coefficient during boiling of nanofluids on smooth, rough and porous coated tubes is proposed. The correlation includes all tested variables in dimensionless form and is valid for low heat flux, i.e., below 100 kW/m2.

  20. Titania sol-gel coatings with silver on non-porous titanium and titanium alloys

    NASA Astrophysics Data System (ADS)

    Horkavcova, D.; Cerny, M.; Sanda, L.; Novak, P.; Jablonska, E.; Zlamalova-Cflova, Z.; Helebrant, A.

    2016-04-01

    The objective of the work was to prepare and characterize titania sol-gel coatings on non-porous titanium and newly developed titanium alloys. Basic titania sol contained two forms of silver. Titania sol without silver was used as a reference sample. Coatings were prepared by dip-coating technique during stirring and fired. Coatings after firing were characterized by scanning electron microscopy. All titania coatings were measured to determine their adhesive and bactericidal properties. Adhesion of the coatings to the substrate was measured by tape test. Gram-negative bacteria E. coli was used for the bactericidal test. Coated substrates were immersed into suspension of E. coli in physiological solution for 24 hours. The in vitro cytotoxicity test was performed after one day. The bactericidal effect without toxicity was confirmed for selected coatings.

  1. Design of Highly Photofunctional Porous Polymer Films with Controlled Thickness and Prominent Microporosity.

    PubMed

    Gu, Cheng; Huang, Ning; Wu, Yang; Xu, Hong; Jiang, Donglin

    2015-09-21

    Porous organic polymers allow the integration of various π-units into robust porous π-networks, but they are usually synthesized as unprocessable solids with poor light-emitting performance as a result of aggregation-related excitation dissipation. Herein, we report a general strategy for the synthesis of highly emissive photofunctional porous polymer films on the basis of a complementary scheme for the structural design of aggregation-induced-emissive π-systems. We developed a high-throughput and facile method for the direct synthesis of large-area porous thin films at the liquid-electrode interface. The approach enables the preparation of microporous films within only a few seconds or minutes and allows precise control over their thickness with sub-nanometer precision. By virtue of rapid photoinduced electron transfer, the thin films can detect explosives with enhanced sensitivity to low parts-per-million levels in a selective manner. PMID:26234636

  2. Design of Highly Photofunctional Porous Polymer Films with Controlled Thickness and Prominent Microporosity

    PubMed Central

    Gu, Cheng; Huang, Ning; Wu, Yang; Xu, Hong; Jiang, Donglin

    2015-01-01

    Porous organic polymers allow the integration of various π-units into robust porous π-networks, but they are usually synthesized as unprocessable solids with poor light-emitting performance as a result of aggregation-related excitation dissipation. Herein, we report a general strategy for the synthesis of highly emissive photofunctional porous polymer films on the basis of a complementary scheme for the structural design of aggregation-induced-emissive π-systems. We developed a high-throughput and facile method for the direct synthesis of large-area porous thin films at the liquid–electrode interface. The approach enables the preparation of microporous films within only a few seconds or minutes and allows precise control over their thickness with sub-nanometer precision. By virtue of rapid photoinduced electron transfer, the thin films can detect explosives with enhanced sensitivity to low parts-per-million levels in a selective manner. PMID:26234636

  3. Osteostatin-coated porous titanium can improve early bone regeneration of cortical bone defects in rats.

    PubMed

    van der Stok, Johan; Lozano, Daniel; Chai, Yoke Chin; Amin Yavari, Saber; Bastidas Coral, Angela P; Verhaar, Jan A N; Gómez-Barrena, Enrique; Schrooten, Jan; Jahr, Holger; Zadpoor, Amir A; Esbrit, Pedro; Weinans, Harrie

    2015-05-01

    A promising bone graft substitute is porous titanium. Porous titanium, produced by selective laser melting (SLM), can be made as a completely open porous and load-bearing scaffold that facilitates bone regeneration through osteoconduction. In this study, the bone regenerative capacity of porous titanium is improved with a coating of osteostatin, an osteoinductive peptide that consists of the 107-111 domain of the parathyroid hormone (PTH)-related protein (PTHrP), and the effects of this osteostatin coating on bone regeneration were evaluated in vitro and in vivo. SLM-produced porous titanium received an alkali-acid-heat treatment and was coated with osteostatin through soaking in a 100 nM solution for 24 h or left uncoated. Osteostatin-coated scaffolds contained ∼0.1 μg peptide/g titanium, and in vitro 81% was released within 24 h. Human periosteum-derived osteoprogenitor cells cultured on osteostatin-coated scaffolds did not induce significant changes in osteogenic (alkaline phosphatase [ALP], collagen type 1 [Col1], osteocalcin [OCN], runt-related transcription factor 2 [Runx2]), or angiogenic (vascular endothelial growth factor [VEGF]) gene expression; however, it resulted in an upregulation of osteoprotegerin (OPG) gene expression after 24 h and a lower receptor activator of nuclear factor kappa-B ligand (RankL):OPG mRNA ratio. In vivo, osteostatin-coated, porous titanium implants increased bone regeneration in critical-sized cortical bone defects (p=0.005). Bone regeneration proceeded until 12 weeks, and femurs grafted with osteostatin-coated implants and uncoated implants recovered, respectively, 66% and 53% of the original femur torque strength (97±31 and 77±53 N·mm, not significant). In conclusion, the osteostatin coating improved bone regeneration of porous titanium. This effect was initiated after a short burst release and might be related to the observed in vitro upregulation of OPG gene expression by osteostatin in osteoprogenitor

  4. Sputtered coatings for protection of spacecraft polymers

    NASA Technical Reports Server (NTRS)

    Banks, B. A.; Mirtich, M. J.; Rutledge, S. K.; Swec, D. M.

    1983-01-01

    Kapton polyimide oxidizes at significant rates (4.3x10(-24) gram/incident oxygen atom) when exposed in low Earth orbit to the ram atomic oxygen flux. Ion beam sputter deposited thin films of Al2O3 and SiO2 as well as a codeposited mixture of predominantly SiO2 with a small amount of polytetrafluoroethylene were evaluated and found to be effective in protecting Kapton from oxidation in both laboratory plasma ashing tests as well as in space on board shuttle flight STS-8. A protective film of or = 96 percent SiO2 and or = 4 percent polytetrafluoroethylene was found to be very flexible compared to the pure metal oxide coatings and resulted in mass loss rates that were 0.2 percent of that of the unprotected Kapton. The optical properties of Kapton for wavelengths investigated between 0.33 and 2.2 microns were not significantly altered by the presence of the coatings or changed by exposure of the coated Kapton to the low Earth orbital ram environment.

  5. Bioinspired porous octacalcium phosphate/silk fibroin composite coating materials prepared by electrochemical deposition.

    PubMed

    Yang, Ya; Wang, Hui; Yan, Feng-Yi; Qi, Yu; Lai, Yue-Kun; Zeng, Dong-Mei; Chen, Guoqiang; Zhang, Ke-Qin

    2015-03-18

    The biomimetic structure and composition of biomaterials are recognized as critical factors that determine their biological performance. A bioinspired nano-micro structured octacalcium phosphate (OCP)/silk fibroin (SF) composite coating on titanium was achieved through a mild electrochemically induced deposition method. Findings indicate that SF plays a critical role in constructing the unique biomimetic hierarchical structure of OCP/SF composite coating layers. In vitro cell culture tests demonstrate that the presence of OCP/SF composite coatings, with highly ordered and hierarchically porous structure, greatly enhance cellular responses. The coatings developed in this study have considerable potential for various hard tissue engineering and applications. PMID:25734421

  6. Porous networks derived from synthetic polymer-clay complexes

    SciTech Connect

    Carrado, K.A.; Thiyagarajan, P.; Elder, D.L.

    1995-05-12

    Synthetic hectorites were hydrothermally crystallized with direct incorporation of a cationic polymer poly(dimethyl diallyl ammonium chloride) (PDDA), and two neutral cellulosic polymers hydroxypropyl methylcellulose (HPMC) and hydroxyethyl cellulose (HEC). Synthetic PDDA-hectorite displays the lowest d-spacing at 15.8 {Angstrom} along with less polymer incorporation (7.8 wt % organic) than the neutral polymers (18--22 wt % organic). Thermal analysis and small angle neutron scattering were used to further examine the polymer-clay systems. Clay platelets of the largest size and best stacking order occur when cationic PDDA polymer is used. PDDA also enhances these properties over the crystallites prepared for a control mineral, where no polymer is used. HEC acts to aggregate the silica, leaving less to react to form clay. The clay platelets which result from HEC are small, not stacked to a large degree, and oriented randomly. Neutral HPMC acts more like cationic PDDA in that larger clay platelets are allowed to form. The extended microstructure of the clay network remains undisturbed after polymer is removed by calcination. When no polymer is used, the synthetic hectorite has a N{sub 2} BET surface area of 200 M{sup 2}/gm, even after calcination. This increases by 20--50% for the synthetic polymer-hectorites after the polymer is removed by calcination.

  7. Adhesion of preceramic inorganic polymer coatings to carbon fibers

    SciTech Connect

    Chaudhry, T.M.; Drzal, L.T.; Ho, H.; Laine, R.

    1996-12-31

    To determine whether the preceramic inorganic polymer coating can provide not only the thermal oxidative protection during both processing and use in metal matrix composites or ceramic matrix composites but also the appropriate composite properties, it is desirable to know how and at what point in the thermal processing cycle the coating-carbon fiber interface undergoes changes that affect the interfacial adhesion and failure mode. Also, it is important to identify the locus of interfacial failure i.e. between fiber and coating or between coating and matrix. This work is directed at determining the interfacial changes and the locus of failure in order to optimize both the coating chemistry and the conversion process. The characteristics of the benchmark interface coating material, silicon oxycarbide, SiO{sub x}C{sub y} or black glass have been studied. SiO{sub x}C{sub y} was chosen because (1) SiO{sub x}C{sub y} is amorphous, (2) it is possible to prepare very well-defined materials, where the chemistry and the evolution of the material with time and temperature are known in detail, and (3) SiO{sub x}C{sub y} is a matrix material used in commercial composites. It has been shown that these coatings are effective in increasing the oxidation resistance of the carbon fibers themselves.

  8. Water-thinnable polymers for durable coatings for different materials

    NASA Astrophysics Data System (ADS)

    Jankowski, Piotr; Kijowska, Dorota

    2014-05-01

    The methods of obtaining water-thinnable polymers - water-thinnable unsaturated polyester resins (WTUPR) - by polycondensation were elaborate and optimized. As hydrophilic monomers different types of sulfonate monomers were used. The monomers, with sulfonate groups and other reactive groups, were obtained by sulfonation of organic compounds with satisfactory yield. All products were analyzed by 1H NMR and 13C NMR spectra. WTUPR were used as polymeric binders for coatings applications. Coatings with relatively high pendulum hardness, good properties and durability, useful for practical applications, were obtained. Typical existing equipment for the production of unsaturated polyester resins can be applied for the industrial preparation of WTUPR.

  9. Water-thinnable polymers for durable coatings for different materials

    SciTech Connect

    Jankowski, Piotr Kijowska, Dorota

    2014-05-15

    The methods of obtaining water-thinnable polymers - water-thinnable unsaturated polyester resins (WTUPR) - by polycondensation were elaborate and optimized. As hydrophilic monomers different types of sulfonate monomers were used. The monomers, with sulfonate groups and other reactive groups, were obtained by sulfonation of organic compounds with satisfactory yield. All products were analyzed by {sup 1}H NMR and {sup 13}C NMR spectra. WTUPR were used as polymeric binders for coatings applications. Coatings with relatively high pendulum hardness, good properties and durability, useful for practical applications, were obtained. Typical existing equipment for the production of unsaturated polyester resins can be applied for the industrial preparation of WTUPR.

  10. Systems and strippable coatings for decontaminating structures that include porous material

    DOEpatents

    Fox, Robert V.; Avci, Recep; Groenewold, Gary S.

    2011-12-06

    Methods of removing contaminant matter from porous materials include applying a polymer material to a contaminated surface, irradiating the contaminated surface to cause redistribution of contaminant matter, and removing at least a portion of the polymer material from the surface. Systems for decontaminating a contaminated structure comprising porous material include a radiation device configured to emit electromagnetic radiation toward a surface of a structure, and at least one spray device configured to apply a capture material onto the surface of the structure. Polymer materials that can be used in such methods and systems include polyphosphazine-based polymer materials having polyphosphazine backbone segments and side chain groups that include selected functional groups. The selected functional groups may include iminos, oximes, carboxylates, sulfonates, .beta.-diketones, phosphine sulfides, phosphates, phosphites, phosphonates, phosphinates, phosphine oxides, monothio phosphinic acids, and dithio phosphinic acids.

  11. Gas chromatographic separation of nitrogen, oxygen, argon, and carbon monoxide using custom-made porous polymers from high purity divinylbenzene

    NASA Technical Reports Server (NTRS)

    Pollock, G. E.; Ohara, D.; Hollis, O. L.

    1984-01-01

    Existing porous polymers were surveyed for their ability to separate the subject gases. Certain products that showed more promise than others were synthesized and the existing synthetic procedures studied and modified to produce new polymers with enhanced ability to separate the subject gases. Evaluation of the porous polymers was carried out practically by gas chromatography at ambient temperature. The modified synthetic procedures were somewhat simpler than the originals. The new porous polymers made with high purity divinylbenzene enabled use of shorter columns to obtain the separations desired.

  12. Solid polymer electrolyte composite membrane comprising laser micromachined porous support

    DOEpatents

    Liu, Han; LaConti, Anthony B.; Mittelsteadt, Cortney K.; McCallum, Thomas J.

    2011-01-11

    A solid polymer electrolyte composite membrane and method of manufacturing the same. According to one embodiment, the composite membrane comprises a rigid, non-electrically-conducting support, the support preferably being a sheet of polyimide having a thickness of about 7.5 to 15 microns. The support has a plurality of cylindrical pores extending perpendicularly between opposing top and bottom surfaces of the support. The pores, which preferably have a diameter of about 5 microns, are made by laser micromachining and preferably are arranged in a defined pattern, for example, with fewer pores located in areas of high membrane stress and more pores located in areas of low membrane stress. The pores are filled with a first solid polymer electrolyte, such as a perfluorosulfonic acid (PFSA) polymer. A second solid polymer electrolyte, which may be the same as or different than the first solid polymer electrolyte, may be deposited over the top and/or bottom of the first solid polymer electrolyte.

  13. Debonding of porous coating of a threaded acetabular component: retrieval analysis.

    PubMed

    Łapaj, Łukasz; Markuszewski, Jacek; Rybak, Tomasz; Wierusz-Kozłowska, Małgorzata

    2013-01-01

    This report presents a case of debonding of plasma sprayed porous titanium coating from a threaded acetabular component which caused aseptic loosening of the implant. Weight bearing after delamination caused abrasive damage of the acetabular shell, and particles of the coating embedded in the acetabular liner. Microscopic examination of periprosthetic tissues showed presence of metal particles and macrophage infiltration. Despite microscopic examination of the retrieved component the cause of debonding remains unclear. PMID:23127634

  14. Process optimization of ultrasonic spray coating of polymer films.

    PubMed

    Bose, Sanjukta; Keller, Stephan S; Alstrøm, Tommy S; Boisen, Anja; Almdal, Kristoffer

    2013-06-11

    In this work we have performed a detailed study of the influence of various parameters on spray coating of polymer films. Our aim is to produce polymer films of uniform thickness (500 nm to 1 μm) and low roughness compared to the film thickness. The coatings are characterized with respect to thickness, roughness (profilometer), and morphology (optical microscopy). Polyvinylpyrrolidone (PVP) is used to do a full factorial design of experiments with selected process parameters such as temperature, distance between spray nozzle and substrate, and speed of the spray nozzle. A mathematical model is developed for statistical analysis which identifies the distance between nozzle and substrate as the most significant parameter. Depending on the drying of the sprayed droplets on the substrate, we define two broad regimes, "dry" and "wet". The optimum condition of spraying lies in a narrow window between these two regimes, where we obtain a film of desired quality. Both with increasing nozzle-substrate distance and temperature, the deposition moves from a wet state to a dry regime. Similar results are also achieved for solvents with low boiling points. Finally, we study film formation during spray coating with poly (D,L-lactide) (PDLLA). The results confirm the processing knowledge obtained with PVP and indicate that the observed trends are identical for spraying of other polymer films. PMID:23631433

  15. Enhanced transport of Si-coated nanoscale zero-valent iron particles in porous media.

    PubMed

    HonetschlÄgerová, Lenka; Janouškovcová, Petra; Kubal, Martin

    2016-01-01

    Laboratory column experiments were conducted to evaluate the effect of previously described silica coating method on the transport of nanoscale zero-valent iron (nZVI) in porous media. The silica coating method showed the potential to prevent the agglomeration of nZVI. Transport experiments were conducted using laboratory-scale sand-packed columns at conditions that were very similar of natural groundwater. Transport properties of non-coated and silica-coated nZVI are investigated in columns of 40 cm length, which were filled with porous media. A suspension was injected in three different Fe particle concentrations (100, 500, and 1000 mg/L) at flow 5  mL/min. Experimental results were compared using nanoparticle attachment efficiency and travel distances which were calculated by classical particle filtration theory. It was found that non-coated particles were essentially immobile in porous media. In contrast, silica-coated particles showed significant transport distances at the tested conditions. Results of this study suggest that silica can increase nZVI mobility in the subsurface. PMID:26582314

  16. Multipurpose Polymeric Coating for Functionalizing Inert Polymer Surfaces.

    PubMed

    Özçam, A Evren; Efimenko, Kirill; Spontak, Richard J; Fischer, Daniel A; Genzer, Jan

    2016-03-01

    In this work, we report on the development of a highly functionalizable polymer coating prepared by the chemical coupling of trichlorosilane (TCS) to the vinyl groups of poly(vinylmethyl siloxane) (PVMS). The resultant PVMS-TCS copolymer can be coated as a functional organic primer layer on a variety of polymeric substrates, ranging from hydrophilic to hydrophobic. Several case studies demonstrating the remarkable and versatile properties of PVMS-TCS coatings are presented. In particular, PVMS-TCS is found to serve as a convenient precursor for the deposition of organosilanes and the subsequent growth of polymer brushes, even on hydrophobic surfaces, such as poly(ethylene terephthalate) and polypropylene. In this study, the physical and chemical characteristics of these versatile PVMS-TCS coatings are interrogated by an arsenal of experimental probes, including scanning electron microscopy, water contact-angle measurements, ellipsometry, Fourier-transform infrared spectroscopy, X-ray photoelectron spectroscopy, and near-edge X-ray absorption fine structure spectroscopy. PMID:26814561

  17. Shear Rheology of Suspensions of Porous Zeolite Particles in Concentrated Polymer Solutions

    NASA Astrophysics Data System (ADS)

    Olanrewaju, Kayode O.; Breedveld, Victor

    2008-07-01

    We present experimental data on the shear rheology of Ultem (polyetherimide)/NMP(l-methyl-2-pyrrolidinone) solutions with and without suspended surface-modified porous/nonporous zeolite (ZSM-5) particles. We found that the porous zeolite suspensions have relative viscosities that significantly exceed the Krieger-Dougherty predictions for hard sphere suspensions. The major origin of this discrepancy is the selective absorption of NMP solvent into the zeolite pores, which raises both the polymer concentration and the particle volume fraction, thus enhancing both the viscosity of the continuous phase Ultem/NMP polymer solution and the particle contribution to the suspension viscosity. Other factors, such as zeolite non-sphericity and specific interactions with Ultem polymer, contribute to the suspension viscosity to a lesser extent. We propose a predictive model for the viscosity of porous zeolite suspensions by incorporating an absorption parameter, α, into the Krieger-Dougherty model. We also propose independent approaches to determine α. The first one is indirect and based on zeolite density/porosity data, assuming that all pores will be filled with solvent. The other method is based on our experimental data, by comparing the viscosity data of porous versus non-porous zeolite suspensions. The different approaches are compared.

  18. Design of sustained release fine particles using two-step mechanical powder processing: particle shape modification of drug crystals and dry particle coating with polymer nanoparticle agglomerate.

    PubMed

    Kondo, Keita; Ito, Natsuki; Niwa, Toshiyuki; Danjo, Kazumi

    2013-09-10

    We attempted to prepare sustained release fine particles using a two-step mechanical powder processing method; particle-shape modification and dry particle coating. First, particle shape of bulk drug was modified by mechanical treatment to yield drug crystals suitable for the coating process. Drug crystals became more rounded with increasing rotation speed, which demonstrates that powerful mechanical stress yields spherical drug crystals with narrow size distribution. This process is the result of destruction, granulation and refinement of drug crystals. Second, the modified drug particles and polymer coating powder were mechanically treated to prepare composite particles. Polymer nanoparticle agglomerate obtained by drying poly(meth)acrylate aqueous dispersion was used as a coating powder. The porous nanoparticle agglomerate has superior coating performance, because it is completely deagglomerated under mechanical stress to form fine fragments that act as guest particles. As a result, spherical drug crystals treated with porous agglomerate were effectively coated by poly(meth)acrylate powder, showing sustained release after curing. From these findings, particle-shape modification of drug crystals and dry particle coating with nanoparticle agglomerate using a mechanical powder processor is expected as an innovative technique for preparing controlled-release coated particles having high drug content and size smaller than 100 μm. PMID:23796831

  19. Porous polymer film calcium ion chemical sensor and method of using the same

    DOEpatents

    Porter, M.D.; Chau, L.K.

    1991-02-12

    A method of measuring calcium ions is disclosed wherein a calcium sensitive reagent, calcichrome, is immobilized on a porous polymer film. The reaction of the calcium sensitive reagent to the Ca(II) is then measured and concentration determined as a function of the reaction. 1 figure.

  20. Enhanced stability of uncemented canine femoral components by bone ingrowth into the porous coatings.

    PubMed

    Jasty, M; Bragdon, C R; Zalenski, E; O'Connor, D; Page, A; Harris, W H

    1997-01-01

    The following questions were answered in this study: (1) What is the initial stability of proximally porous-coated canine femoral components? (2) Does bone ingrowth occur under these conditions? (3) Is the stability enhanced by tissue ingrowth in vivo? The stability of proximally porous-coated femoral components of canine total hip arthroplasties after 6 months to 2 years of in vivo service in dogs was measured in vitro using displacement transducers under loads simulating canine midstance. This was compared with the stability of identical components under the same loading conditions immediately after implantation in vitro in the contralateral femurs. The femurs were then sectioned and bone ingrowth into the porous coatings was quantified. The results showed that immediately after implantation the implants can move as much as 50 microns, but that the bone ingrowth into porous coatings of canine femoral components can occur even under such conditions. These data also suggested that the relative motion existing at the time of insertion can be reduced to very small amounts (< 10 microns) by bone ingrowth. PMID:9021510

  1. Effects of microstructure on the corrosion behavior of CoCr porous coatings on orthopedic implants.

    PubMed

    Placko, H E; Brown, S A; Payer, J H

    1998-02-01

    Cobalt-chromium alloy porous coatings have become increasingly popular as a means of achieving a stable, longer lasting fixation on orthopedic implants. However, sintering heat treatments cause changes in the microstructure that result in changes in the corrosion behavior of the porous coatings. Experiments were conducted to examine the effects of microstructure on the corrosion of CoCr porous coatings. Four distinct microstructures were characterized. Light microscopy revealed microstructures A and B had relatively fewer carbides and a large-grain structure, microstructures C and D displayed a finer grain size with significant carbide formation, predominantly within grains and fusion zones. Accelerated anodic corrosion experiments were conducted to study the localized attack of each microstructure. Experiments were conducted using metallographically polished porous-coated disks for durations of 1, 4, 16, 24, and 72 h. The disks were examined with SEM and EDS to observe preferential attack and element depletion. Results showed a progressive dissolution of the matrix, with preferential attack of the grain boundaries and regions adjacent to the carbides due to sensitization. A precipitation layer was found to be Cr-rich and possibly composed of chromium hydroxide or a chromium orthophosphate. In addition, the solution became yellow in color with longer exposure times, possibly due to the presence of chromate ions, as indicated by an increased chromium level detected by AAS. PMID:9457560

  2. Porous low modulus Ti40Nb compacts with electrodeposited hydroxyapatite coating for biomedical applications.

    PubMed

    Zhuravleva, K; Chivu, A; Teresiak, A; Scudino, S; Calin, M; Schultz, L; Eckert, J; Gebert, A

    2013-05-01

    Porous ß-type non-toxic Ti40Nb alloy was prepared by compaction of mechanically alloyed powder mixed with NaCl or Mg particles as space-holder material. The compacts with porosity of 36-80% demonstrated a very low Young's modulus of ~1.5-3 GPa and compression strength of ~10-35 MPa, which is suitable for potential implant material application. Porous samples were electrochemically covered with hydroxyapatite. The influence of the deposition time and of the electrolyte concentrations on the morphology of the hydroxyapatite coating was studied. It is demonstrated that a homogenous coating of hydroxyapatite crystals with different shape and size can be obtained on the surface of the porous samples. PMID:23498259

  3. Interfacial Behavior of Polymer Coated Nanoparticle

    NASA Astrophysics Data System (ADS)

    Qi, Luqing; Shamsijazeyi, Hadi; Mann, Jason; Verduzco, Rafael; Hirasaki, George; Rice University Team

    2015-03-01

    Oxidized carbon black (OCB) nanoparticle is functionalized with different coatings, i.e. alkyl group, polyvinyl alcohol (PVA) and partially sulfonated polyvinyl alcohol (sPVA). In oil and water systems, the functionalized nanoparticle is found to have a versatile dispersion i.e. in lower aqueous phase, in upper oil phase, or in middle phase microemulsion. Oil substitute n-octane and commercial oil IOSPAR have been test as oil phase; series of commercially available surfactant, C12-4,5 orthoxylene sulfonate(OXS), i-C13-(PO)7 -SO4Na (S13B), surfactant blend of anionic Alfoterra with nonionic Tergitol have been test as additive to help with the OCB dispersion. It is found that the OCB with sulfonated polyvinyl alcohol attachment (sPVA-OCB) stays in microemulsion; with the increase of salinity, it follows the microemulsion to go from lower phase, to middle phase, and to upper phase. The dispersion of sPVA and alkyl functionalized OCB (Cn-OCB-sPVA) is the balance of the length of alkyl and sPVA and the degree of sulfonation of PVA, depending on which, it can either disperse into microemulsion or form a separate layer. The sPVA-OCB also indicates a tolerance of high salinity; this is shown by the stable dispersion of it in blend surfactant solution of anionic Alfoterra and nonionic Tergitol at high salinity API brine(8% NaCl and 2% CaCl2). The study of different functionality on OCB dispersion can help design appropriate modified nanoparticle as additive for enhanced oil recovery either to reduce the interfacial tension between oil and water, or to stabilize microemulsion.

  4. In vitro and in vivo evaluations of 3D porous TCP-coated and non-coated alumina scaffolds.

    PubMed

    Kim, Young-Hee; Anirban, Jyoti M; Song, Ho-Yeon; Seo, Hyung-Seok; Lee, Byong-Taek

    2011-02-01

    Both tricalcium phosphate (TCP) and alumina have been extensively studied and shown to have high biocompatibility. Tricalcium phosphate has improved biodegradability and a higher solubility than hydroxyapatite. In contrast, alumina (Al(2)O(3)) is almost completely inert at physiological conditions and has been used as a biomaterial due to its wear resistance, high surface finish, and excellent hardness. Thus, the combination of these two implants would result in greater biocompatibility and phenotype maintenance. A polyurethane (PU) foam replica method was employed in this study to coat TCP on an alumina scaffold. The TCP-coated alumina scaffold was then sintered to generate a porous surface morphology. The pore sizes obtained using this approach ranged between 100-600 µm, which is ideal for cellular proliferation. The cytotoxicity, cellular proliferation, differentiation, and ECM deposition on the coated scaffold resulted in longer-term viability of osteogenic markers compared to the non-coated scaffold. Moreover, the osteogenic properties of porous TCP-coated Al(2)O(3) scaffolds were reported in this study using rabbit models. The TCP/Al(2)O( 3) scaffold and control Al(2)O(3) scaffolds were implanted in the rabbit femur. The bone tissue response was analyzed with micro-computed tomography (micro CT) at 12 and 24 weeks after implantation. The porous scaffolds exhibited favorable hard and soft tissue responses at both time points. At 24 weeks, a three-fold increase in bone tissue ingrowth was observed in defects containing TCP-coated Al(2)O(3) scaffolds compared to control Al(2)O(3) scaffolds. PMID:20207781

  5. Osteoconductivity and osteoinductivity of porous hydroxyapatite coatings deposited by liquid precursor plasma spraying: in vivo biological response study.

    PubMed

    Huang, Yi; He, Jing; Gan, Lu; Liu, Xiaoguang; Wu, Yao; Wu, Fang; Gu, Zhong-wei

    2014-12-01

    The beneficial effect of a porous structure on the biological functions of calcium phosphate bulk ceramic or scaffold has been well documented. Nevertheless, the effect of a porous structure on the in vivo performance of hydroxyapatite (HA) coatings has been rarely reported, partly due to the difficulty in synthesizing porous HA coatings suitable for commercial applications. In this study, we have carried out a systematic in vivo study of porous HA-coated Ti implants (with and without surface modification) prepared by the liquid precursor plasma spraying process, in terms of its osteoconductivity and osteoinductivity. The results suggest the clear advantage of the porous structure over the dense structure, despite the pore structure (about 48% porosity and less than 100 μm average pore size) being far from the ideal pore structure reported for bulk ceramic. The porous HA-coated implant significantly promotes early bone ingrowth at the pre-generated defective region, and early fixation at the bone-implant interface, especially at early implantation time (one month), showing about 120% and 40% increases respectively over those of the dense HA-coated implants prepared by the conventional atmospheric plasma spraying process. Moreover, the porous structure can be readily used to incorporate collagen/rh-BMP2, which demonstrates clear ectopic bone formation. Overall, the results suggest the augmentation of bone ingrowth is significant for HA coatings with a porous structure, which is critical for the early fixation and long-term stability of medical implants. PMID:25384201

  6. Erosion Resistant Coatings for Polymer Matrix Composites in Propulsion Applications

    NASA Technical Reports Server (NTRS)

    Sutter, James K.; Naik, Subhash K.; Horan, Richard; Miyoshi, Kazuhisa; Bowman, Cheryl; Ma, Kong; Leissler, George; Sinatra, Raymond; Cupp, Randall

    2003-01-01

    Polymer Matrix Composites (PMCs) offer lightweight and frequently low cost alternatives to other materials in many applications. High temperature PMCs are currently used in limited propulsion applications replacing metals. Yet in most cases, PMC propulsion applications are not in the direct engine flow path since particulate erosion degrades PMC component performance and therefore restricts their use in gas turbine engines. This paper compares two erosion resistant coatings (SANRES and SANPRES) on PMCs that are useful for both low and high temperature propulsion applications. Collaborating over a multi-year period, researchers at NASA Glenn Research Center, Allison Advanced Developed Company, and Rolls-Royce Corporation have optimized these coatings in terms of adhesion, surface roughness, and erosion resistance. Results are described for vigorous hot gas/particulate erosion rig and engine testing of uncoated and coated PMC fan bypass vanes from the AE 3007 regional jet gas turbine engine. Moreover, the structural durability of these coatings is described in long-term high cycle fatigue tests. Overall, both coatings performed well in all tests and will be considered for applications in both commercial and defense propulsion applications.

  7. Size-selective yolk-shell nanoreactors with nanometer-thin porous polymer shells.

    PubMed

    Jia, Ying; Shmakov, Sergey N; Register, Paul; Pinkhassik, Eugene

    2015-09-01

    Yolk-shell nanoreactors with metal nanoparticle core and ultrathin porous polymer shells are effective catalysts for heterogeneous reactions. Polymer shells provide size-selectivity and improved reusability of catalyst. Nanocapsules with single-nanometer porous shells are prepared by vesicle-templated directed assembly. Metal nanoparticles are formed either by selective initiation in pre-fabricated nanocapsules or simultaneously with the creation of a crosslinked polymer shell. In this study, we investigated the oxidation of benzyl alcohol and benzaldehyde catalyzed by gold nanoparticles and hydrogenation of cyclohexene catalyzed by platinum nanoparticles. Comparison of newly created nanoreactors with commercially available nanoparticles revealed superior reusability and size selectivity in nanoreactors while showing no negative effect on reaction kinetics. PMID:26223572

  8. Electrodeposition of porous hydroxyapatite/calcium silicate composite coating on titanium for biomedical applications

    NASA Astrophysics Data System (ADS)

    Huang, Yong; Han, Shuguang; Pang, Xiaofeng; Ding, Qionqion; Yan, Yajing

    2013-04-01

    A novel method of electrolytic porous hydroxyapatite/calcium silicate (HA/CaSiO3) composite coating was conducted on pure titanium in a mixed solution of nano-SiO2, Ca(NO3)2 and NH4H2PO4. SEM observation showed that the composite layer was porous, thereby providing abundant sites for the osteoblast adhesion. XRD results showed that the composite coating was mainly composed of HA and CaSiO3. Bond strength testing exhibited that HA-CaSiO3/Ti had higher bond strength than HA/Ti. The HA/CaSiO3 coating was more corrosion resistant than the HA coating based on the polarization tests. In vitro cell experiments demonstrated that both the HA and HA/CaSiO3 coatings showed better cell response than the bared titanium. In addition, the proliferation of MC3T3-E1 osteoblast cells grown on the HA/CaSiO3 coating were remarkably higher than those on the bared Ti and pure HA coating.

  9. Soluble porous coordination polymers by mechanochemistry: from metal-containing films/membranes to active catalysts for aerobic oxidation.

    PubMed

    Zhang, Pengfei; Li, Haiying; Veith, Gabriel M; Dai, Sheng

    2015-01-14

    Soluble porous coordination polymers from mechanochemical synthesis are presented through a coordination polymerization between highly contorted, rigid tetraphenol and a broad variety of transition metal ions. These polymers can be easily cast as metal-containing films or freestanding membranes. Importantly, as-made coordination polymers are highly active and stable in the aerobic oxidation of allylic C-H bonds. PMID:25389070

  10. Solid polymer electrolyte composite membrane comprising plasma etched porous support

    DOEpatents

    Liu, Han; LaConti, Anthony B.

    2010-10-05

    A solid polymer electrolyte composite membrane and method of manufacturing the same. According to one embodiment, the composite membrane comprises a rigid, non-electrically-conducting support, the support preferably being a sheet of polyimide having a thickness of about 7.5 to 15 microns. The support has a plurality of cylindrical pores extending perpendicularly between opposing top and bottom surfaces of the support. The pores, which preferably have a diameter of about 0.1 to 5 microns, are made by plasma etching and preferably are arranged in a defined pattern, for example, with fewer pores located in areas of high membrane stress and more pores located in areas of low membrane stress. The pores are filled with a first solid polymer electrolyte, such as a perfluorosulfonic acid (PFSA) polymer. A second solid polymer electrolyte, which may be the same as or different than the first solid polymer electrolyte, may be deposited over the top and/or bottom of the first solid polymer electrolyte.

  11. Porous nickel MCFC cathode coated by potentiostatically deposited cobalt oxide. I. A structural and morphological study

    NASA Astrophysics Data System (ADS)

    Escudero, M. J.; Rodrigo, T.; Mendoza, L.; Cassir, M.; Daza, L.

    Porous nickel cathode was protected by potentiostatically deposited cobalt at different experimental conditions: oxidation potential and electrolysis duration. The deposition growth increased with the oxidation potential yielding a more developed granular structure with smaller grains. Thin layers of Co 3O 4 were identified by X-ray diffraction (XRD) and Raman spectroscopy. CoOOH was detected by X-ray photoelectron spectroscopy (XPS) before annealing treatment and Co 3O 4 after heating the sample at 500 °C during 4 h in air. After this treatment, some morphological changes were observed on the coated samples due to grain compaction and oxidation of the nickel substrate. The porosity of the coated samples was relatively close to that of the sole porous nickel. These coatings exhibited an appropriate dual-pore structure with macro and micro pores, a basic MCFC requirement.

  12. A novel approach to a fine particle coating using porous spherical silica as core particles.

    PubMed

    Ishida, Makoto; Uchiyama, Jumpei; Isaji, Keiko; Suzuki, Yuta; Ikematsu, Yasuyuki; Aoki, Shigeru

    2014-08-01

    Abstract The applicability of porous spherical silica (PSS) was evaluated as core particles for pharmaceutical products by comparing it with commercial core particles such as mannitol (NP-108), sucrose and microcrystalline cellulose spheres. We investigated the physical properties of core particles, such as particle size distribution, flow properties, crushing strength, plastic limit, drying rate, hygroscopic property and aggregation degree. It was found that PSS was a core particle of small particle size, low friability, high water adsorption capacity, rapid drying rate and lower occurrence of particle aggregation, although wettability is a factor to be carefully considered. The aggregation and taste-masking ability using PSS and NP-108 as core particles were evaluated at a fluidized-bed coating process. The functional coating under the excess spray rate shows different aggregation trends and dissolution profiles between PSS and NP-108; thereby, exhibiting the formation of uniform coating under the excess spray rate in the case of PSS. This expands the range of the acceptable spray feed rates to coat fine particles, and indicates the possibility of decreasing the coating time. The results obtained in this study suggested that the core particle, which has a property like that of PSS, was useful in overcoming such disadvantages as large particle size, which feels gritty in oral cavity; particle aggregation; and the long coating time of the particle coating process. These results will enable the practical fine particle coating method by increasing the range of optimum coating conditions and decreasing the coating time in fluidized bed technology. PMID:23781858

  13. Selective surface-enhanced Raman spectroscopy using a polymer-coated substrate

    SciTech Connect

    Pal, A.; Stokes, D.L.; Alarie, J.P.; Vo-Dinh, T.

    1995-09-15

    The polymer, poly(vinylpyrrolidone), is investigated as a potential coating for alumina-based surface-enhanced Raman scattering (SERS) substrates. Description for dip-coating alumina substrates with a 5% (w/v) methanolic solution of the polymer is included. Using these polymer-coated substrates, various compounds, including monocyclic aromatic compounds with hydroxyl, carboxyl, and various nitrogen-based functional groups, are detected. Intensity of SERS signals from the polymer-coated substrates in comparison to that of SERS signals from uncoated substrates is demonstrated to be a function of the analyte permeability to the polymer coating. Different enhancement factors are reported for various compounds, such as benzoic acid, isonicotinic acid, and 2,4-dinitrophenol, thus indicating some enhancement selectivity of the polymer coating to various analytes. Using benzoic acid as a test compound, various coating procedures (horizontal and vertical dipping procedures) have been evaluated. The poly(vinylpyrrolidone)-coated substrate is shown to yield a relative standard deviation in SERS signal intensity of approximately 20%. The potential of the polymer-coated substrate as a selective detection probe is illustrated using the analyses of binary mixtures. Finally, the advantages of the polymer coating for protecting the SERS-active layer are also discussed. 29 refs., 7 figs., 1 tab.

  14. Development of a porous polymer pH optrode.

    PubMed

    Liu, J N; Shahriari, M R; Sigel, G H

    1992-12-15

    A novel fiber-optic pH sensor has been developed with long-term stability and high sensitivity. The sensor is based on a porous cellulose triacetate fiber immobilized with Congo Red (pH indicator). This intrinsic fiberoptic pH sensor has shown excellent sensitivity, reversibility, and stability. It has also been demonstrated that the pH optrode is immune to metal-ion interferences. PMID:19798326

  15. Porous biomorphic silicon carbide ceramics coated with hydroxyapatite as prospective materials for bone implants.

    PubMed

    Gryshkov, Oleksandr; Klyui, Nickolai I; Temchenko, Volodymyr P; Kyselov, Vitalii S; Chatterjee, Anamika; Belyaev, Alexander E; Lauterboeck, Lothar; Iarmolenko, Dmytro; Glasmacher, Birgit

    2016-11-01

    Porous and cytocompatible silicon carbide (SiC) ceramics derived from wood precursors and coated with bioactive hydroxyapatite (HA) and HA-zirconium dioxide (HA/ZrO2) composite are materials with promising application in engineering of bone implants due to their excellent mechanical and structural properties. Biomorphic SiC ceramics have been synthesized from wood (Hornbeam, Sapele, Tilia and Pear) using a forced impregnation method. The SiC ceramics have been coated with bioactive HA and HA/ZrO2 using effective gas detonation deposition approach (GDD). The surface morphology and cytotoxicity of SiC ceramics as well as phase composition and crystallinity of deposited coatings were analyzed. It has been shown that the porosity and pore size of SiC ceramics depend on initial wood source. The XRD and FTIR studies revealed the preservation of crystal structure and phase composition of in the HA coating, while addition of ZrO2 to the initial HA powder resulted in significant decomposition of the final HA/ZrO2 coating and formation of other calcium phosphate phases. In turn, NIH 3T3 cells cultured in medium exposed to coated and uncoated SiC ceramics showed high re-cultivation efficiency as well as metabolic activity. The recultivation efficiency of cells was the highest for HA-coated ceramics, whereas HA/ZrO2 coating improved the recultivation efficiency of cells as compared to uncoated SiC ceramics. The GDD method allowed generating homogeneous HA coatings with no change in calcium to phosphorus ratio. In summary, porous and cytocompatible bio-SiC ceramics with bioactive coatings show a great promise in construction of light, robust, inexpensive and patient-specific bone implants for clinical application. PMID:27524006

  16. Electrochemical coating of dental implants with anodic porous titania for enhanced osteointegration

    PubMed Central

    Shayganpour, Amirreza; Rebaudi, Alberto; Cortella, Pierpaolo; Diaspro, Alberto

    2015-01-01

    Summary Clinical long-term osteointegration of titanium-based biomedical devices is the main goal for both dental and orthopedical implants. Both the surface morphology and the possible functionalization of the implant surface are important points. In the last decade, following the success of nanostructured anodic porous alumina, anodic porous titania has also attracted the interest of academic researchers. This material, investigated mainly for its photocatalytic properties and for applications in solar cells, is usually obtained from the anodization of ultrapure titanium. We anodized dental implants made of commercial grade titanium under different experimental conditions and characterized the resulting surface morphology with scanning electron microscopy equipped with an energy dispersive spectrometer. The appearance of nanopores on these implants confirm that anodic porous titania can be obtained not only on ultrapure and flat titanium but also as a conformal coating on curved surfaces of real objects made of industrial titanium alloys. Raman spectroscopy showed that the titania phase obtained is anatase. Furthermore, it was demonstrated that by carrying out the anodization in the presence of electrolyte additives such as magnesium, these can be incorporated into the porous coating. The proposed method for the surface nanostructuring of biomedical implants should allow for integration of conventional microscale treatments such as sandblasting with additive nanoscale patterning. Additional advantages are provided by this material when considering the possible loading of bioactive drugs in the porous cavities. PMID:26665091

  17. Fabrication and Characterization of a Porous Silicon Drug Delivery System with an Initiated Chemical Vapor Deposition Temperature-Responsive Coating.

    PubMed

    McInnes, Steven J P; Szili, Endre J; Al-Bataineh, Sameer A; Vasani, Roshan B; Xu, Jingjing; Alf, Mahriah E; Gleason, Karen K; Short, Robert D; Voelcker, Nicolas H

    2016-01-12

    This paper reports on the fabrication of a pSi-based drug delivery system, functionalized with an initiated chemical vapor deposition (iCVD) polymer film, for the sustainable and temperature-dependent delivery of drugs. The devices were prepared by loading biodegradable porous silicon (pSi) with a fluorescent anticancer drug camptothecin (CPT) and coating the surface with temperature-responsive poly(N-isopropylacrylamide-co-diethylene glycol divinyl ether) (pNIPAM-co-DEGDVE) or non-stimulus-responsive poly(aminostyrene) (pAS) via iCVD. CPT released from the uncoated oxidized pSi control with a burst release fashion (∼21 nmol/(cm(2) h)), and this was almost identical at temperatures both above (37 °C) and below (25 °C) the lower critical solution temperature (LCST) of the switchable polymer used, pNIPAM-co-DEGDVE (28.5 °C). In comparison, the burst release rate from the pSi-pNIPAM-co-DEGDVE sample was substantially slower at 6.12 and 9.19 nmol/(cm(2) h) at 25 and 37 °C, respectively. The final amount of CPT released over 16 h was 10% higher at 37 °C compared to 25 °C for pSi coated with pNIPAM-co-DEGDVE (46.29% vs 35.67%), indicating that this material can be used to deliver drugs on-demand at elevated temperatures. pSi coated with pAS also displayed sustainable drug delivery profiles, but these were independent of the release temperature. These data show that sustainable and temperature-responsive delivery systems can be produced by functionalization of pSi with iCVD polymer films. Benefits of the iCVD approach include the application of the iCVD coating after drug loading without causing degradation of the drug commonly caused by exposure to factors such as solvents or high temperatures. Importantly, the iCVD process is applicable to a wide array of surfaces as the process is independent of the surface chemistry and pore size of the nanoporous matrix being coated. PMID:26654169

  18. In vivo integrity of polymer-coated gold nanoparticles

    NASA Astrophysics Data System (ADS)

    Kreyling, Wolfgang G.; Abdelmonem, Abuelmagd M.; Ali, Zulqurnain; Alves, Frauke; Geiser, Marianne; Haberl, Nadine; Hartmann, Raimo; Hirn, Stephanie; de Aberasturi, Dorleta Jimenez; Kantner, Karsten; Khadem-Saba, Gülnaz; Montenegro, Jose-Maria; Rejman, Joanna; Rojo, Teofilo; de Larramendi, Idoia Ruiz; Ufartes, Roser; Wenk, Alexander; Parak, Wolfgang J.

    2015-07-01

    Inorganic nanoparticles are frequently engineered with an organic surface coating to improve their physicochemical properties, and it is well known that their colloidal properties may change upon internalization by cells. While the stability of such nanoparticles is typically assayed in simple in vitro tests, their stability in a mammalian organism remains unknown. Here, we show that firmly grafted polymer shells around gold nanoparticles may degrade when injected into rats. We synthesized monodisperse radioactively labelled gold nanoparticles (198Au) and engineered an 111In-labelled polymer shell around them. Upon intravenous injection into rats, quantitative biodistribution analyses performed independently for 198Au and 111In showed partial removal of the polymer shell in vivo. While 198Au accumulates mostly in the liver, part of the 111In shows a non-particulate biodistribution similar to intravenous injection of chelated 111In. Further in vitro studies suggest that degradation of the polymer shell is caused by proteolytic enzymes in the liver. Our results show that even nanoparticles with high colloidal stability can change their physicochemical properties in vivo.

  19. Reducing protein adsorption with polymer-grafted hyaluronic acid coatings.

    PubMed

    Ramadan, Mohamed H; Prata, Joseph E; Karácsony, Orsolya; Dunér, Gunnar; Washburn, Newell R

    2014-07-01

    We report a thermoresponsive chemical modification strategy of hyaluronic acid (HA) for coating onto a broad range of biomaterials without relying on chemical functionalization of the surface. Poly(di(ethylene glycol) methyl ether methacrylate) (PMEO2MA), a polymer with a lower critical solution temperature of 26 °C in water, was grafted onto HA to allow facile formation of biopolymer coatings. While the mechanism for film formation appears to involve a complex combination of homogeneous nucleation followed by heterogeneous film growth, we demonstrate that it resulted in hydrophilic coatings that significantly reduce protein adsorption despite the high fraction of hydrophobic (PMEO2MA). Structural characterization was performed using atomic force microscopy (AFM), which showed the formation of a dense, continuous coating based on 200 nm domains that were stable in protein solutions for at least 15 days. The coatings had a water contact angle of 16°, suggesting the formation of hydrophilic but not fully wetting films. Quartz crystal microbalance with dissipation monitoring (QCM-D) as well as biolayer interferometry (BLI) techniques were used to measure adsorption of bovine serum albumin (BSA), fibrinogen (Fbg), and human immunoglobulin (IgG), with results indicating that HA-PMEO2MA-coated surfaces effectively inhibited adsorption of all three serum proteins. These results are consistent with previous studies demonstrating that this degree of hydrophilicity is sufficient to generate an effectively nonfouling surface and suggest that segregation during the solubility transition resulted in a surface that presented the hydrophilic HA component of the hybrid biopolymer. We conclude that PMEO2MA-grafted HA is a versatile platform for the passivation of hydrophobic biomaterial surfaces without need for substrate functionalization. PMID:24892924

  20. Flow reduction in microchannels coated with a polymer brush.

    PubMed

    Lanotte, Luca; Guido, Stefano; Misbah, Chaouqi; Peyla, Philippe; Bureau, Lionel

    2012-09-25

    We report on the design of microchannels made of glass capillary coated with polymer brushes elaborated by the so-called "grafting-from" technique. We present measurements of velocity profiles for pressure-driven flows of water in such "hairy" capillaries. We show that the flow reduction induced by the presence of the brush is unexpectedly greater than what could be anticipated from simple geometric arguments on the reduction of the effective capillary diameter or from predictions by models describing the brush layer as a poro-elastic boundary. PMID:22935030

  1. Polymer Replicas of Photonic Porous Silicon for Sensing and Drug Delivery Applications

    NASA Astrophysics Data System (ADS)

    Li, Yang Yang; Cunin, Frédérique; Link, Jamie R.; Gao, Ting; Betts, Ronald E.; Reiver, Sarah H.; Chin, Vicki; Bhatia, Sangeeta N.; Sailor, Michael J.

    2003-03-01

    Elaborate one-dimensional photonic crystals are constructed from a variety of organic and biopolymers, which can be dissolved or melted, by templating the solution-cast or injection-molded materials in porous silicon or porous silicon dioxide multilayer (rugate dielectric mirror) structures. After the removal of the template by chemical dissolution, the polymer castings replicate the photonic features and the nanostructure of the master. We demonstrate that these castings can be used as vapor sensors, as deformable and tunable optical filters, and as self-reporting, bioresorbable materials.

  2. Polymer replicas of photonic porous silicon for sensing and drug delivery applications.

    PubMed

    Li, Yang Yang; Cunin, Frédérique; Link, Jamie R; Gao, Ting; Betts, Ronald E; Reiver, Sarah H; Chin, Vicki; Bhatia, Sangeeta N; Sailor, Michael J

    2003-03-28

    Elaborate one-dimensional photonic crystals are constructed from a variety of organic and biopolymers, which can be dissolved or melted, by templating the solution-cast or injection-molded materials in porous silicon or porous silicon dioxide multilayer (rugate dielectric mirror) structures. After the removal of the template by chemical dissolution, the polymer castings replicate the photonic features and the nanostructure of the master. We demonstrate that these castings can be used as vapor sensors, as deformable and tunable optical filters, and as self-reporting, bioresorbable materials. PMID:12663921

  3. Biocompatible two-layer tantalum/titania-polymer hybrid coating.

    PubMed

    Cortecchia, Elisa; Pacilli, Annalisa; Pasquinelli, Gianandrea; Scandola, Mariastella

    2010-09-13

    Using a two-step procedure, radiopaque and biocompatible coatings were obtained, consisting of a tantalum layer deposited by sputtering technique and of an upper organic-inorganic hybrid layer synthesized via sol-gel. As shown by radiographic images, tantalum confers to plastic substrates good X-ray visibility, adjustable via control of deposition time, but its adhesion to the substrate is poor and manipulation easily damages the metal layer. Polymer-titania hybrid coatings, synthesized using poly-ε-caprolactone (PCL) or carboxy-terminated polydimethylsiloxane (PDMS) as organic precursors, were applied on the metal layer as biocompatible protective coatings. Biocompatibility is demonstrated by cytotoxicity tests conducted using vascular wall resident-mesenchymal stem cells (VW-MSCs). Both coatings show very good adhesion to the substrate, showing no sign of detachment upon large substrate deformations. Under such conditions, SEM observations show that the PCL-containing hybrid forms cracks, whereas the PDMS-based hybrid does not crack, suggesting possible applications of the latter material as a protective layer of sputtered tantalum radiopaque markers for flexible medical devices. PMID:20831278

  4. Surface dynamics and mechanics in liquid crystal polymer coatings

    NASA Astrophysics Data System (ADS)

    Liu, Danqing; Broer, Dirk J.

    2015-03-01

    Based on liquid crystal networks we developed `smart' coatings with responsive surface topographies. Either by prepatterning or by the formation of self-organized structures they can be switched on and off in a pre-designed manner. Here we provide an overview of our methods to generate coatings that form surface structures upon the actuation by light. The coating oscillates between a flat surface and a surface with pre-designed 3D micro-patterns by modulating a light source. With recent developments in solid state lighting, light is an attractive trigger medium as it can be integrated in a device for local control or can be used remotely for flood or localized exposure. The basic principle of formation of surface topographies is based on the change of molecular organization in ordered liquid crystal polymer networks. The change in order leads to anisotropic dimensional changes with contraction along the director and expansion to the two perpendicular directions and an increase in volume by the formation of free volume. These two effects work in concert to provide local expansion and contraction in the coating steered by the local direction of molecular orientation. The surface deformation, expressed as the height difference between the activated regions and the non-activated regions divided by the initial film thickness, is of the order of 20%. Switching occurs immediately when the light is switched `on' and `off' and takes several tens of seconds.

  5. Universal hydrophilic coating of thermoplastic polymers currently used in microfluidics.

    PubMed

    Zilio, Caterina; Sola, Laura; Damin, Francesco; Faggioni, Lucia; Chiari, Marcella

    2014-02-01

    A number of materials used to fabricate disposable microfluidic devices are hydrophobic in nature with water contact angles on their surface ranging from 80° to over 100°. This characteristic makes them unsuitable for a number of microfluidic applications. Both the wettability and analyte adsorption parameters are highly dependent on the surface hydrophobicity. In this article, we propose a general method to coat the surface of five materials: polydimethylsiloxane (PDMS), cyclic olefin copolymer (COC), polyethylene terephthalate (PET), polycarbonate (PC), and polytetrafluoroethylene (PTFE). This fast and robust process, which is easily implementable in any laboratory including microfabrication clean room facilities, was devised by combining gas-phase and wet chemical modification processes. Two different coatings that improve the surface hydrophilicity were prepared via the "dip and rinse" approach by immersing the plasma oxidized materials into an aqueous solution of two different poly(dimethylacrylamide) copolymers incorporating a silane moiety and functionalized with either N-acryloyloxysuccinimide (NAS) (poly(DMA-NAS-MAPS) or glycidyl methacrylate (GMA) (poly(DMA-GMA-MAPS). The coating formation was confirmed by contact angle (CA) analysis comparing the variation of CAs of uncoated and coated surfaces subjected to different aging treatments. The antifouling character of the polymer was demonstrated by fluorescence and interferometric detection of proteins adsorbed on the surafce. This method is of great interest in microfluidics due to its broad applicability to a number of materials with varying chemical compositions. PMID:24037663

  6. Click Chemistry Immobilization of Antibodies on Polymer Coated Gold Nanoparticles.

    PubMed

    Finetti, Chiara; Sola, Laura; Pezzullo, Margherita; Prosperi, Davide; Colombo, Miriam; Riva, Benedetta; Avvakumova, Svetlana; Morasso, Carlo; Picciolini, Silvia; Chiari, Marcella

    2016-07-26

    The goal of this work is to develop an innovative approach for the coating of gold nanoparticles (AuNPs) with a synthetic functional copolymer. This stable coating with a thickness of few nanometers provides, at the same time, stabilization and functionalization of the particles. The polymeric coating consists of a backbone of polydimethylacrylamide (DMA) functionalized with an alkyne monomer that allows the binding of azido modified molecules by Cu(I)-catalyzed azide/alkyne 1,3-dipolar cycloaddition (CuAAC, click chemistry). The thin polymer layer on the surface stabilizes the colloidal suspension whereas the alkyne functions pending from the backbone are available for the reaction with azido-modified proteins. The reactivity of the coating is demonstrated by immobilizing an azido modified anti-mouse IgG antibody on the particle surface. This approach for the covalent binding of antibody to a gold-NPs is applied to the development of gold labels in biosensing techniques. PMID:27367748

  7. Mechanisms of chain adsorption on porous substrates and critical conditions of polymer chromatography.

    PubMed

    Cimino, Richard T; Rasmussen, Christopher J; Brun, Yefim; Neimark, Alexander V

    2016-11-01

    Polymer adsorption is a ubiquitous phenomenon with numerous technological and healthcare applications. The mechanisms of polymer adsorption on surfaces and in pores are complex owing to a competition between various entropic and enthalpic factors. Due to adsorption of monomers to the surface, the chain gains in enthalpy yet loses in entropy because of confining effects. This competition leads to the existence of critical conditions of adsorption when enthalpy gain and entropy loss are in balance. The critical conditions are controlled by the confining geometry and effective adsorption energy, which depends on the solvent composition and temperature. This phenomenon has important implications in polymer chromatography, since the retention at the critical point of adsorption (CPA) is chain length independent. However, the mechanisms of polymer adsorption in pores are poorly understood and there is an ongoing discussion in the theoretical literature about the very existence of CPA for polymer adsorption on porous substrates. In this work, we examine the mechanisms of chain adsorption on a model porous substrate using Monte Carlo (MC) simulations. We distinguish three adsorption mechanisms depending on the chain location: on external surface, completely confined in pores, and also partially confined in pores in so-called "flower" conformations. The free energies of different conformations of adsorbed chains are calculated by the incremental gauge cell MC method that allows one to determine the partition coefficient as a function of the adsorption potential, pore size, and chain length. We confirm the existence of the CPA for chain length independent separation on porous substrates, which is explained by the dominant contributions of the chain adsorption at the external surface, in particular in flower conformations. Moreover, we show that the critical conditions for porous and nonporous substrates are identical and depend only on the surface chemistry. The theoretical

  8. Surface characterisation and electrochemical behaviour of porous titanium dioxide coated 316L stainless steel for orthopaedic applications

    NASA Astrophysics Data System (ADS)

    Nagarajan, S.; Rajendran, N.

    2009-01-01

    Porous titanium dioxide was coated on surgical grade 316L stainless steel (SS) and its role on the corrosion protection and enhanced biocompatibility of the materials was studied. X-ray diffraction analysis (XRD), atomic force microscopy (AFM), Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM) and energy dispersive X-ray analysis (EDAX) were carried out to characterise the surface morphology and also to understand the structure of the as synthesised coating on the substrates. The corrosion behaviour of titanium dioxide coated samples in simulated body fluid was evaluated using polarisation and impedance spectroscopy studies. The results reveal that the titanium dioxide coated 316L SS exhibit a higher corrosion resistance than the uncoated 316L SS. The titanium dioxide coated surface is porous, uniform and also it acts as a barrier layer to metallic substrate and the porous titanium dioxide coating induces the formation of hydroxyapatite layer on the metal surface.

  9. Effect of the properties of a porous coating on boundary layer stability. [considering porous slates

    NASA Technical Reports Server (NTRS)

    Gaponov, S. A.

    1978-01-01

    Drawing off gas from the boundary layer is a well-known method for increasing the stability of boundary layers. The increase in stability is primarily connected with a change in the velocity profile form in the case of suction. On the basis of the assumption that the velocity perturbations on a porous slate do not equal zero, the influence of the properties of a permeable surface upon the boundary layer stability were studied.

  10. Versatile surface engineering of porous nanomaterials with bioinspired polyphenol coatings for targeted and controlled drug delivery

    NASA Astrophysics Data System (ADS)

    Li, Juan; Wu, Shuxian; Wu, Cuichen; Qiu, Liping; Zhu, Guizhi; Cui, Cheng; Liu, Yuan; Hou, Weijia; Wang, Yanyue; Zhang, Liqin; Teng, I.-Ting; Yang, Huang-Hao; Tan, Weihong

    2016-04-01

    The development of biocompatible drug delivery systems with targeted recognition and controlled release has experienced a number of design challenges, including, for example, complicated preparation steps and premature drug release. Herein, we address these problems through an in situ self-polymerization method that synthesizes biodegradable polyphenol-coated porous nanomaterials for targeted and controlled drug delivery. As a proof of concept, we synthesized polyphenol-coated mesoporous silica nanoparticles, termed MSN@polyphenol. The polyphenol coatings not only improved colloidal stability and prevented premature drug leakage, but also provided a scaffold for immobilization of targeting moieties, such as aptamers. Both immobilization of targeting aptamers and synthesis of polyphenol coating are easily accomplished without the aid of any other organic reagents. Importantly, the polyphenol coating (EGCg) used in this study could be biodegraded by acidic pH and intracellular glutathione, resulting in the release of trapped anticancer drugs. Based on confocal fluorescence microscopy and cytotoxicity experiments, drug-loaded and polyphenol-coated MSNs were shown to possess highly efficient internalization and an apparent cytotoxic effect on target cancer, but not control, cells. Our results suggest that these highly biocompatible and biodegradable polyphenol-coated MSNs are promising vectors for controlled-release biomedical applications and cancer therapy.The development of biocompatible drug delivery systems with targeted recognition and controlled release has experienced a number of design challenges, including, for example, complicated preparation steps and premature drug release. Herein, we address these problems through an in situ self-polymerization method that synthesizes biodegradable polyphenol-coated porous nanomaterials for targeted and controlled drug delivery. As a proof of concept, we synthesized polyphenol-coated mesoporous silica nanoparticles

  11. Bioinspired porous membranes containing polymer nanoparticles for wound healing.

    PubMed

    Ferreira, Ana M; Mattu, Clara; Ranzato, Elia; Ciardelli, Gianluca

    2014-12-01

    Skin damages covering a surface larger than 4 cm(2) require a regenerative strategy based on the use of appropriate wound dressing supports to facilitate the rapid tissue replacement and efficient self-healing of the lost or damaged tissue. In the present work, A novel biomimetic approach is proposed for the design of a therapeutic porous construct made of poly(L-lactic acid) (PLLA) fabricated by thermally induced phase separation (TIPS). Biomimicry of ECM was achieved by immobilization of type I collagen through a two-step plasma treatment for wound healing. Anti-inflammatory (indomethacin)-containing polymeric nanoparticles (nps) were loaded within the porous membranes in order to minimize undesired cell response caused by post-operative inflammation. The biological response to the scaffold was analyzed by using human keratinocytes cell cultures. In this work, a promising biomimetic construct for wound healing and soft tissue regeneration with drug-release properties was fabricated since it shows (i) proper porosity, pore size, and mechanical properties, (ii) biomimicry of ECM, and (iii) therapeutic potential. PMID:24522948

  12. Effect of glycerol-L-lactide coating polymer on bone ingrowth of bFGF-coated hydroxyapatite implants.

    PubMed

    Alt, Volker; Pfefferle, Hans-Joachim; Kreuter, Jörg; Stahl, Jens-Peter; Pavlidis, Theodoros; Meyer, Christof; Mockwitz, Jürgen; Wenisch, Sabine; Schnettler, Reinhard

    2004-09-14

    Basic fibroblast growth factor (bFGF)-coated hydroxyapatite (HA) cylinders showed good bony incorporation in a previously conducted animal study. However, some cylinders exhibited focal inhomogeneous bone ingrowth. The purpose of the current study was to test whether glycerol-L-lactide polymer coating could improve release properties and bone incorporation of bFGF-coated HA implants. bFGF-coated HA cylinders with or without coating polymer were investigated for in vitro release of bFGF by an immuno-ligand-assay and also for bone ingrowth in miniature pigs after 42 and 84 days. Release from bFGF polymer composites was lower for the first 3 days compared to the other group but was more homogenous and detectable amounts were still found after 20 days. There was significant delay in bone ingrowth of the polymer implants in which even after 84 days bone ingrowth was not completed, whereas in the other group incorporation after 42 days occurred. Detailed histology revealed filling of the HA pores with the polymer, making ingrowth of the surrounding host bone impossible. Only after 84 days starting resorption of the polymer accompanied by bone ingrowth was found. The current study showed that glycerol-L-lactide is not suitable for coating of HA implants due to polymer induced "locking" of HA pores. PMID:15342184

  13. Palladium coated porous anodic alumina membranes for gas reforming processes

    NASA Astrophysics Data System (ADS)

    Wu, Jeremy P.; Brown, Ian W. M.; Bowden, Mark E.; Kemmitt, Timothy

    2010-11-01

    Nanostructured ceramic membranes with ultrathin coatings of palladium metal have been demonstrated to separate hydrogen gas from a gas mixture containing nitrogen with 10% carbon dioxide and 10% hydrogen at temperatures up to 550 °C. The mechanically robust and thermally durable membranes were fabricated using a combination of conventional and high-efficiency anodisation processes on high purity aluminium foils. A pH-neutral plating solution has also been developed to enable electroless deposition of palladium metal on templates which were normally prone to chemical corrosion in strong acid or base environment. Activation and thus seeding of palladium nuclei on the surface of the template were essential to ensure uniform and fast deposition, and the thickness of the metal film was controlled by time of deposition. The palladium coated membranes showed improved hydrogen selectivity with increased temperature as well as after prolonged exposure to hydrogen, demonstrating excellent potential for gas separation technologies.

  14. Distributed Pore Chemistry in Porous Organic Polymers in Tissue Culture Flasks

    NASA Technical Reports Server (NTRS)

    Koontz, Steven L. (Inventor)

    1999-01-01

    A method for making a biocompatible polymer article using a uniform atomic oxygen treatment is disclose. The substrate may be subsequently optionally grated with a compatibilizing compound. Compatibilizing compounds may include proteins, phosphorylcholine groups, platelet adhesion preventing polymers, albumin adhesion promoters, and the like. The compatibilized substrate may also have a living cell layer adhered thereto. The atomic oxygen is preferably produced by a flowing afterglow microwave discharge, wherein the substrate resides in a sidearm out of the plasma. Also, methods for culturing cells for various purposes using the various membranes are disclosed as well. Also disclosed are porous organic polymers having a distributed pore chemistry (DPC) comprising hydrophilic and hydrophobic regions, and a method for making the DPC by exposing the polymer to atomic oxygen wherein the rate of hydrophilization is greater than the rate of mass loss.

  15. Porous α-Al2O3 thermal barrier coatings with dispersed Pt particles prepared by cathode plasma electrolytic deposition

    NASA Astrophysics Data System (ADS)

    Wang, Peng; He, Ye-dong; Deng, Shun-jie; Zhang, Jin

    2016-01-01

    Porous α-Al2O3 thermal barrier coatings (TBCs) containing dispersed Pt particles were prepared by cathode plasma electrolytic deposition (CPED). The influence of the Pt particles on the microstructure of the coatings and the CPED process were studied. The prepared coatings were mainly composed of α-Al2O3. The average thickness of the coatings was approximately 100 μm. Such single-layer TBCs exhibited not only excellent high-temperature cyclic oxidation and spallation resistance, but also good thermal insulation properties. Porous α-Al2O3 TBCs inhibit further oxidation of alloy substrates because of their extremely low oxygen diffusion rate, provide good thermal insulation because of their porous structure, and exhibit excellent mechanical properties because of the toughening effect of the Pt particles and because of stress relaxation induced by deformation of the porous structure.

  16. Dynamics of polymer film formation during spin coating

    NASA Astrophysics Data System (ADS)

    Mouhamad, Y.; Mokarian-Tabari, P.; Clarke, N.; Jones, R. A. L.; Geoghegan, M.

    2014-09-01

    Standard models explaining the spin coating of polymer solutions generally fail to describe the early stages of film formation, when hydrodynamic forces control the solution behavior. Using in situ light scattering alongside theoretical and semi-empirical models, it is shown that inertial forces (which initially cause a vertical gradient in the radial solvent velocity within the film) play a significant role in the rate of thinning of the solution. The development of thickness as a function of time of a solute-free liquid (toluene) and a blend of polystyrene and poly(methyl methacrylate) cast from toluene were fitted to different models as a function of toluene partial pressure. In the case of the formation of the polymer blend film, a concentration-dependent (Huggins) viscosity formula was used to account for changes in viscosity during spin coating. A semi-empirical model is introduced, which permits calculation of the solvent evaporation rate and the temporal evolution of the solute volume fraction and solution viscosity.

  17. Dynamics of polymer film formation during spin coating

    SciTech Connect

    Mouhamad, Y.; Clarke, N.; Jones, R. A. L.; Geoghegan, M.; Mokarian-Tabari, P.

    2014-09-28

    Standard models explaining the spin coating of polymer solutions generally fail to describe the early stages of film formation, when hydrodynamic forces control the solution behavior. Using in situ light scattering alongside theoretical and semi-empirical models, it is shown that inertial forces (which initially cause a vertical gradient in the radial solvent velocity within the film) play a significant role in the rate of thinning of the solution. The development of thickness as a function of time of a solute-free liquid (toluene) and a blend of polystyrene and poly(methyl methacrylate) cast from toluene were fitted to different models as a function of toluene partial pressure. In the case of the formation of the polymer blend film, a concentration-dependent (Huggins) viscosity formula was used to account for changes in viscosity during spin coating. A semi-empirical model is introduced, which permits calculation of the solvent evaporation rate and the temporal evolution of the solute volume fraction and solution viscosity.

  18. Prognostic Significance of Polymer Coatings in Zotarolimus-Eluting Stents.

    PubMed

    Iqbal, M Bilal; Nadra, Imad J; Din, Jehangir N; Hendry, Cara; Ding, Lillian; Fung, Anthony; Aymong, Eve; Chan, Albert W; Hodge, Steven; Robinson, Simon D; Della Siega, Anthony

    2016-03-01

    Polymer coatings on drug-eluting stents (DES) serve as a vehicle for delivery of antirestenotic drugs. Whether they influence outcomes for contemporary DES is unknown. The evolution of polymer coatings for zotarolimus-eluting stents (ZES) provides a natural experiment that facilitates such analysis. The Resolute ZES (R-ZES) uses the same antirestenotic drug as the Endeavor ZES (E-ZES) but has a more biocompatible polymer with enhanced drug release kinetics. However, there are limited data on the real-world comparative efficacy of R-ZES and the preceding E-ZES. Thus, we analyzed 17,643 patients who received either E-ZES or R-ZES from 2008 to 2014 from the British Columbia Cardiac Registry. A total of 9,869 patients (56%) received E-ZES and 7,774 patients (44%) received R-ZES. Compared with E-ZES, R-ZES was associated with lower 2-year mortality (4.1% vs 6.4%, p <0.001) and 2-year target vessel revascularization (TVR; 6.8% vs 10.7%, p <0.001). R-ZES use was an independent predictor of lower mortality rate and TVR. This was confirmed in propensity-matched analyses for 2-year mortality (hazard ratio [HR] 0.59, 95% CI 0.49 to 0.71, p <0.001) and 2-year TVR (HR 0.86, 95% CI 0.75 to 0.98, p = 0.032). Instrumental variable analyses demonstrated R-ZES to be associated with lower 2-year mortality (Δ = -2.2%, 95% CI -4.3% to -0.2%, p = 0.032) and 2-year TVR (Δ = -3.3% to 95% CI -6.1% to -0.7%, p = 0.015). Acknowledging the limitations of observational analyses, this study has shown that R-ZES was associated with lower long-term TVR and mortality. These data are reassuring for the newer R-ZES and demonstrate how polymer coatings may influence the clinical performance of DES with wider implications for future DES development and design. PMID:26796194

  19. High-performance antireflective coatings with a porous nanoparticle layer for visible wavelengths.

    PubMed

    Murata, Tsuyoshi; Ishizawa, Hitoshi; Tanaka, Akira

    2011-03-20

    Ghosts and flares are well-known problems that are caused by reflections from lens surfaces when we take photographs. It is more difficult to prevent such stray light in a digital camera than in a film camera because of high reflectance from the low-pass filter and diffraction from the image sensor. To prevent such stray light, we introduce an ultralow refractive index layer into the antireflective (AR) coatings. We used the solgel method to form porous fluoride layers with ultralow refractive indices, and we succeeded in developing a unique process to form AR coatings with superior performance. PMID:21460972

  20. Effect of nano-hydroxyapatite coating on the osteoinductivity of porous biphasic calcium phosphate ceramics

    PubMed Central

    2014-01-01

    Background Porous biphasic calcium phosphate (BCP) ceramics exhibit good biocompatibility and bone conduction but are not inherently osteoinductive. To overcome this disadvantage, we coated conventional porous BCP ceramics with nano-hydroxyapatite (nHA). nHA was chosen as a coating material due to its high osteoinductive potential. Methods We used a hydrothermal deposition method to coat conventional porous BCP ceramics with nHA and assessed the effects of the coating on the physical and mechanical properties of the underlying BCP. Next, its effects on mesenchymal stem cell (MSC) attachment, proliferation, viability, and osteogenic differentiation were investigated. Results nHA formed a deposited layer on the BCP surface, and synthesized nHA had a rod-like shape with lengths ranging from ~50–200 nm and diameters from ~15–30 mm. The nHA coating did not significantly affect the density, porosity, flexural strength, or compressive strength of the underlying BCP (P > 0.1). Scanning electron microscopy showed MSC attachment to the scaffolds, with a healthy morphology and anchorage to nHA crystals via cytoplasmic processes. The densities of MSCs attached on BCP and nHA-coated BCP scaffolds were 62 ± 26 cells/mm2 and 63 ± 27 cells/mm2 (P > 0.1), respectively, after 1 day and 415 ± 62 cells/mm2 and 541 ± 35 cells/mm2 (P < 0.05) respectively, after 14 days. According to an MTT assay, MSC viability was higher on nHA-coated BCP scaffolds than on BCP scaffolds (P < 0.05). In addition, MSCs on nHA-coated BCP scaffolds produced more alkaline phosphatase, collagen type I, and osteocalcin than MSCs on BCP scaffolds (P < 0.05). Conclusions Our results demonstrate that BCP scaffolds coated with nHA were more conducive for MSC adhesion, proliferation, and osteogenic differentiation than conventional, uncoated BCP scaffolds, indicating that nHA coating can enhance the osteoinductive potential of BCP ceramics, making this material more

  1. Facile one-pot synthesis of porphyrin based porous polymer networks (PPNs) as biomimetic catalysts

    SciTech Connect

    Zou, LF; Feng, DW; Liu, TF; Chen, YP; Fordham, S; Yuan, S; Tian, J; Zhou, HC

    2015-01-01

    Stable porphyrin based porous polymer networks, PPN-23 and PPN-24, have been synthesized through a facile one-pot approach by the aromatic substitution reactions of pyrrole and aldehydes. PPN-24(Fe) shows high catalytic efficiency as a biomimetic catalyst in the oxidation reaction of 2,2'-azino-bis(3-ethylbenzthiazoline-6-sulfonic acid) (ABTS) in the presence of H2O2.

  2. Synthesis of catalytically active porous organic polymers from metalloporphyrin building blocks

    SciTech Connect

    Shultz, Abraham M.; Farha, Omar K.; Hupp, Joseph T.; Nguyen, SonBinh T.

    2011-04-01

    The synthesis of a porous organic polymer (POP) containing free-base porphyrin subunits has been accomplished by the condensation of a bis(phthalic acid)porphyrin with tetra(4-aminophenyl)methane. Metallation by post-synthesis modification affords microporous materials incorporating either Fe or Mn(porphyrins) that have been shown to be active catalysts for both olefin epoxidation and alkane hydroxylation.

  3. Design of 2D Porous Coordination Polymers Based on Metallacrown Units.

    PubMed

    Atzeri, Corrado; Marchiò, Luciano; Chow, Chun Y; Kampf, Jeff W; Pecoraro, Vincent L; Tegoni, Matteo

    2016-05-01

    A 12-metallacrown-4 (MC) complex was designed and employed as the building block in the synthesis of coordination polymers, one of which is the first permanently porous MC architecture. The connection of the four-fold symmetric MC subunits by Cu(II) nodes led to the formation of 2D layers of metallacrowns. Channels are present in the crystalline architecture, which exhibits permanent porosity manifested in N2 and CO2 uptake capacity. PMID:26951956

  4. Development of Polymer Coatings for the ProSEDS Tether

    NASA Technical Reports Server (NTRS)

    Vaughn, Jason A.; Kamenetsky, Rachel R.; Finckenor, Miria; Wright, Ken

    2000-01-01

    The ProSEDS mission is designed to provide an on-orbit demonstration of the electrodynamic propulsion capabilities of tethers in space. The ProSEDS experiment will be a secondary payload on a Delta 11 unmanned, expendable booster. A 5 km conductive tether is attached to the deployer baseplate on the Delta 11 second stage and collects current from the low Earth orbit (LEO) plasma to facilitate de-orbit of the Delta II second stage. The conductive tether is attached to a 10-15 km non-conductive tether, which in turn is attached to an endmass. A bare metal tether would have the best conductivity but thermal concerns preclude this design. A conductive polymer developed by Triton Systems has been optimized for optimum conductivity and thermo-optical properties. The current design for the ProSEDS conductive tether is seven individually coated strands of 28 AWG aluminum wire, coated with 12.7 micrometers (0.5 mil) atomic oxygen-resistant conductive polymer composed of a mixture of COR and PANi, wrapped around a braided Kevlar 29 core. Extensive testing has been performed at the Marshall Space Flight Center to qualify this material for flight on ProSEDS. Atomic oxygen exposure has been performed, with solar absorptance and infrared emittance measured before and after exposure. Plasma chamber tests have been completed, as well as tether deployment tests. Also developed for the ProSEDS mission was the insulating polymer TOR-BP. Approximately 200 meters of the conductive tether closest to the Delta II second stage is insulated to prevent any electron reconnection to the tether from the plasma contactor. The insulating material is TOR-BP with a dielectric strength of TBD.

  5. Adhesion of E. coli to silver- or copper-coated porous clay ceramic surfaces

    NASA Astrophysics Data System (ADS)

    Yakub, I.; Soboyejo, W. O.

    2012-06-01

    Porous ceramic water filters (CWFs), produced by sintering a mixture of clay and a combustible material (such as woodchips), are often used in point-of-use water filtration systems that occlude microbes by size exclusion. They are also coated with colloidal silver, which serves as a microbial disinfectant. However, the adhesion of microbes to porous clay surfaces and colloidal silver coated clay surfaces has not been studied. This paper presents the results of atomic force microscopy (AFM) measurements of the adhesion force between Escherichia coli bacteria, colloidal silver, and porous clay-based ceramic surfaces. The adhesion of silver and copper nanoparticles is also studied in control experiments on these alternative disinfectant materials. The adhesive force between the wide range of possible bi-materials was measured using pull-off measurements during force microscopy. These were combined with measurements of AFM tip radii/substrate roughness that were incorporated into adhesion models to obtain the adhesion energies for the pair wise interaction. Of the three antimicrobial metals studied, the colloidal silver had the highest affinity for porous ceramic surface (125 ± 32 nN and ˜0.29 J/m2) while the silver nanoparticles had the highest affinity for E. coli bacteria (133 ± 21 nN and ˜0.39 J/m2). The implications of the results are then discussed for the design of ceramic water filter that can purify water by adsorption and size exclusion.

  6. Tailoring of the porous structure of soft emulsion-templated polymer materials.

    PubMed

    Kovalenko, Artem; Zimny, Kévin; Mascaro, Benoit; Brunet, Thomas; Mondain-Monval, Olivier

    2016-06-21

    This paper discusses the formation of soft porous materials obtained by the polymerization of inverse water-in-silicone (polydimethylsiloxane, PDMS) emulsions. We show that the initial state of the emulsion has a strong impact on the porous structure and properties of the final material. We show that using a surfactant with different solubilities in the emulsion continuous phase (PDMS), it is possible to tune the interaction between emulsion droplets, which leads to materials with either interconnected or isolated pores. These two systems present completely different behavior upon drying, which results in macroporous air-filled materials in the interconnected case and in a collapsed material with low porosity in the second case. Finally, we compare the mechanical and acoustical properties of these two types of bulk polymer monoliths. We also describe the formation of micrometric polymer particles (beads) in these two cases. We show that materials with an interconnected macroporous structure have low mechanical moduli and low sound speed, and are suitable for acoustic applications. The mechanical and acoustical properties of the materials with a collapsed porous structure are similar to those of non-porous silicone, which makes them acoustically inactive. PMID:27195990

  7. Revealing Amphiphilic Nanodornains of Anti-Biofouling Polymer Coatings

    SciTech Connect

    Amadei, CA; Yang, R; Chiesa, M; Gleason, KK; Santos, S

    2014-04-09

    Undesired bacterial adhesion and biofilm formation on wetted surfaces leads to significant economic and environmental costs in various industries. Amphiphilic coatings with molecular hydrophilic and hydrophobic patches can mitigate such biofouling effectively in an environmentally friendly manner. The coatings are synthesized by copolymerizing (Hydroxyethyl)methacrylate and perfluorodecylacrylate via initiated chemical vapor deposition (iCVD). In previous studies, the size of the patches was estimated to be similar to 1.4-1.75 nm by fitting protein adsorption data to a theoretical model. However, no direct observations of the molecular heterogeneity exist and therefore the origin of the fouling resistance of amphiphilic coatings remains unclear. Here, the amphiphilic nature is investigated by amplitude modulation atomic force microscopy (AM-AFM). High-resolution images obtained by penetrating and oscillating the AFM tip under the naturally present water layer with sub-nanometer amplitudes reveal, for the first time, the existence of amphiphilic nanodomains (1-2 nm(2)). Compositional heterogeneity at the nanoscale is further corroborated by a statistical analysis on the data obtained with dynamic AM-AFM force spectroscopy. Variations in the long range attractive forces, responsible for water affinity, are also identified. These nanoscopic results on the polymers wettability are also confirmed by contact angle measurements (i.e., static and dynamic). The unprecedented ability to visualize the amphiphilic nanodomains as well as sub-nanometer crystalline structures provides strong evidence for the existence of previously postulated nanostructures, and sheds light on the underlying antifouling mechanism of amphiphilic chemistry.

  8. Fabrication of interpenetrating polymer network chitosan/gelatin porous materials and study on dye adsorption properties.

    PubMed

    Cui, Li; Xiong, Zihao; Guo, Yi; Liu, Yun; Zhao, Jinchao; Zhang, Chuanjie; Zhu, Ping

    2015-11-01

    One kind of adsorbent based on chitosan and gelatin with interpenetrating polymer networks (IPN) and porous dual structures was prepared using genipin as the cross-linker. These dual structures were demonstrated by means of Fourier transform infrared spectroscopy (FT-IR), thermogravimetric analysis (TGA) and scanning electron microscopy (SEM). Adsorptions of acid orange II dye from aqueous solution were carried out at different genipin contents, adsorption times and pH values. The results showed that this material was put up the largest adsorption capacity when the genipin content is 0.25 mmol/L, meanwhile, the lower the solution pH value the greater the adsorption capacity. The chitosan/gelatin interpenetrating polymer networks porous material displayed pH-sensitive and rapidly response in adsorption and desorption to pH altered. It is indicated that the cross-linked chitosan/gelatin interpenetrating polymer networks porous material could be used as a recyclable adsorbent in removal or separation of anionic dyes as environmental pH condition changed. PMID:26256356

  9. Biodegradability of regenerated cellulose films coated with polyurethane/natural polymers interpenetrating polymer networks

    SciTech Connect

    Zhang, L.; Zhou, J.; Huang, J.; Gong, P. Zhou, Q.; Zheng, L.; Du, Y.

    1999-11-01

    Interpenetrating polymer network (IPN) coatings synthesized from castor-oil-based polyurethane (PU) with chitosan, nitrocellulose, or elaeostearin were coated on regenerated cellulose (RC) film for curing at 80--100 C for 2--5 min, providing biodegradable, water-resistant cellulose films coded, respectively, as RCCH, RCNC, and RCEs. The coated films were buried in natural soil for decaying and inoculated with a spore suspension of fungi on the agar medium, respectively, to test biodegradability. The viscosity-average molecular weight, M{sub {eta}}, and the weight of the degraded films decreased sharply with the progress of degradation. The degradation half-lifes, t{sub 1/2}, of the films in soil at 30 C were found to be 19 days for RC, 25 days for RCNC, 32 days for RCCH, and 45 days for the RCEs films. Scanning electron microscopy (SEM) showed that the extent of decay followed in the order RC {gt} RCNC {gt} RCCH {gt} RCEs. SEM, infrared (IR), high-performance liquid chromatography (HPLC), and CO{sub 2} evolution results indicated that the microorganisms directly attacked the water-resistant coating layer and then penetrated into the cellulose to speedily metabolize, while accompanying with producing CO{sub 2}, H{sub 2}O, glucose cleaved from cellulose, and small molecules decomposed from the coatings.

  10. Development of electrically conductive DLC coated stainless steel separators for polymer electrolyte membrane fuel cell

    NASA Astrophysics Data System (ADS)

    Suzuki, Yasuo; Watanabe, Masanori; Toda, Tadao; Fujii, Toshiaki

    2013-06-01

    Polymer electrolyte fuel cell (PEFC) as one of generation devices of electrical power is rapidly expanding the market as clean energy instead of petroleum and atomic energy. Residential fuel cell goes into quantity production and introduction of fuel cell for use in automobiles starts in the year 2015 in Japan. Critical subject for making fuel cell expand is how to reduce cost of fuel cell. In this paper we describe about separator plate which domains large ratio of cost in fuel cell stack. In present time, carbon is used in material of residential fuel cell separator. Metal separators are developed in fuel cell for use in automobiles because of need of mechanical strength at first. In order to make fuel cell expand in market, further cost reduction is required. But the metal separator has problem that by using metal separator contact resistance occurred by metal corrosion increases and catalyst layer and membrane degrade. In recent time we found out to protect from corrosion and dissolution of metals by coating the film of porous free conductive DLC with plasma ion implantation and deposition technology that we have developed. Film of electrically conductive DLC was formed with high speed of 13 μm/hr by ICP plasma, and coating cost breakout was performed.

  11. Compressible Graphene-Coated Polymer Foams with Ultralow Density for Adjustable Electromagnetic Interference (EMI) Shielding.

    PubMed

    Shen, Bin; Li, Yang; Zhai, Wentao; Zheng, Wenge

    2016-03-01

    The fabrication of low-density and compressible polymer/graphene composite (PGC) foams for adjustable electromagnetic interference (EMI) shielding remains a daunting challenge. Herein, ultralightweight and compressible PGC foams have been developed by simple solution dip-coating of graphene on commercial polyurethane (PU) sponges with highly porous network structure. The resultant PU/graphene (PUG) foams had a density as low as ∼0.027-0.030 g/cm(3) and possessed good comprehensive EMI shielding performance together with an absorption-dominant mechanism, possibly due to both conductive dissipation and multiple reflections and scattering of EM waves by the inside 3D conductive graphene network. Moreover, by taking advantage of their remarkable compressibility, the shielding performance of the PUG foams could be simply adjusted through a simple mechanical compression, showing promise for adjustable EMI shielding. We believe that the strategy for fabricating PGC foams through a simple dip-coating method could potentially promote the large-scale production of lightweight foam materials for EMI shielding. PMID:26974443

  12. Honeycomb-like porous gel polymer electrolyte membrane for lithium ion batteries with enhanced safety.

    PubMed

    Zhang, Jinqiang; Sun, Bing; Huang, Xiaodan; Chen, Shuangqiang; Wang, Guoxiu

    2014-01-01

    Lithium ion batteries have shown great potential in applications as power sources for electric vehicles and large-scale energy storage. However, the direct uses of flammable organic liquid electrolyte with commercial separator induce serious safety problems including the risk of fire and explosion. Herein, we report the development of poly(vinylidene difluoride-co-hexafluoropropylene) polymer membranes with multi-sized honeycomb-like porous architectures. The as-prepared polymer electrolyte membranes contain porosity as high as 78%, which leads to the high electrolyte uptake of 86.2 wt%. The PVDF-HFP gel polymer electrolyte membranes exhibited a high ionic conductivity of 1.03 mS cm(-1) at room temperature, which is much higher than that of commercial polymer membranes. Moreover, the as-obtained gel polymer membranes are also thermally stable up to 350 °C and non-combustible in fire (fire-proof). When applied in lithium ion batteries with LiFePO4 as cathode materials, the gel polymer electrolyte demonstrated excellent electrochemical performances. This investigation indicates that PVDF-HFP gel polymer membranes could be potentially applicable for high power lithium ion batteries with the features of high safety, low cost and good performance. PMID:25168687

  13. Honeycomb-like porous gel polymer electrolyte membrane for lithium ion batteries with enhanced safety

    NASA Astrophysics Data System (ADS)

    Zhang, Jinqiang; Sun, Bing; Huang, Xiaodan; Chen, Shuangqiang; Wang, Guoxiu

    2014-08-01

    Lithium ion batteries have shown great potential in applications as power sources for electric vehicles and large-scale energy storage. However, the direct uses of flammable organic liquid electrolyte with commercial separator induce serious safety problems including the risk of fire and explosion. Herein, we report the development of poly(vinylidene difluoride-co-hexafluoropropylene) polymer membranes with multi-sized honeycomb-like porous architectures. The as-prepared polymer electrolyte membranes contain porosity as high as 78%, which leads to the high electrolyte uptake of 86.2 wt%. The PVDF-HFP gel polymer electrolyte membranes exhibited a high ionic conductivity of 1.03 mS cm-1 at room temperature, which is much higher than that of commercial polymer membranes. Moreover, the as-obtained gel polymer membranes are also thermally stable up to 350°C and non-combustible in fire (fire-proof). When applied in lithium ion batteries with LiFePO4 as cathode materials, the gel polymer electrolyte demonstrated excellent electrochemical performances. This investigation indicates that PVDF-HFP gel polymer membranes could be potentially applicable for high power lithium ion batteries with the features of high safety, low cost and good performance.

  14. Honeycomb-like porous gel polymer electrolyte membrane for lithium ion batteries with enhanced safety

    PubMed Central

    Zhang, Jinqiang; Sun, Bing; Huang, Xiaodan; Chen, Shuangqiang; Wang, Guoxiu

    2014-01-01

    Lithium ion batteries have shown great potential in applications as power sources for electric vehicles and large-scale energy storage. However, the direct uses of flammable organic liquid electrolyte with commercial separator induce serious safety problems including the risk of fire and explosion. Herein, we report the development of poly(vinylidene difluoride-co-hexafluoropropylene) polymer membranes with multi-sized honeycomb-like porous architectures. The as-prepared polymer electrolyte membranes contain porosity as high as 78%, which leads to the high electrolyte uptake of 86.2 wt%. The PVDF-HFP gel polymer electrolyte membranes exhibited a high ionic conductivity of 1.03 mS cm−1 at room temperature, which is much higher than that of commercial polymer membranes. Moreover, the as-obtained gel polymer membranes are also thermally stable up to 350°C and non-combustible in fire (fire-proof). When applied in lithium ion batteries with LiFePO4 as cathode materials, the gel polymer electrolyte demonstrated excellent electrochemical performances. This investigation indicates that PVDF-HFP gel polymer membranes could be potentially applicable for high power lithium ion batteries with the features of high safety, low cost and good performance. PMID:25168687

  15. Versatile surface engineering of porous nanomaterials with bioinspired polyphenol coatings for targeted and controlled drug delivery.

    PubMed

    Li, Juan; Wu, Shuxian; Wu, Cuichen; Qiu, Liping; Zhu, Guizhi; Cui, Cheng; Liu, Yuan; Hou, Weijia; Wang, Yanyue; Zhang, Liqin; Teng, I-Ting; Yang, Huang-Hao; Tan, Weihong

    2016-04-21

    The development of biocompatible drug delivery systems with targeted recognition and controlled release has experienced a number of design challenges, including, for example, complicated preparation steps and premature drug release. Herein, we address these problems through an in situ self-polymerization method that synthesizes biodegradable polyphenol-coated porous nanomaterials for targeted and controlled drug delivery. As a proof of concept, we synthesized polyphenol-coated mesoporous silica nanoparticles, termed MSN@polyphenol. The polyphenol coatings not only improved colloidal stability and prevented premature drug leakage, but also provided a scaffold for immobilization of targeting moieties, such as aptamers. Both immobilization of targeting aptamers and synthesis of polyphenol coating are easily accomplished without the aid of any other organic reagents. Importantly, the polyphenol coating (EGCg) used in this study could be biodegraded by acidic pH and intracellular glutathione, resulting in the release of trapped anticancer drugs. Based on confocal fluorescence microscopy and cytotoxicity experiments, drug-loaded and polyphenol-coated MSNs were shown to possess highly efficient internalization and an apparent cytotoxic effect on target cancer, but not control, cells. Our results suggest that these highly biocompatible and biodegradable polyphenol-coated MSNs are promising vectors for controlled-release biomedical applications and cancer therapy. PMID:27050780

  16. Antibacterial ability and osteogenic activity of porous Sr/Ag-containing TiO2 coatings.

    PubMed

    He, Xiaojing; Zhang, Xiangyu; Bai, Long; Hang, Ruiqiang; Huang, Xiaobo; Qin, Lin; Yao, Xiaohong; Tang, Bin

    2016-01-01

    Implant-associated infection and poor osseointegration remains a major clinical challenge in Ti-based implant materials. A versatile strategy to endow Ti-based implants with long-term antibacterial ability as well as better osteogenic activity is highly desirable for high quality implantation. Strontium (Sr) has been shown to be a significant element to favor bone growth by promoting new bone formation and inhibiting bone resorption. In this study, a novel duplex-treatment technique encompassing magnetron sputtering with micro-arc oxidation is utilized to fabricate porous Sr/Ag-containing TiO2 coatings loaded with different concentrations of Ag and Sr. All coatings are porous with pore size less than 5 µm. Ag is primarily distributed homogeneously inside the pores, and the concentrations of Ag in Sr/Ag-containing TiO2 coatings with low and high Ag contents are 0.40 at.% and 0.83 at.% respectively. We have demonstrated that this kind of coating displays long-lasting antibacterial ability even up to 28 d due to the incorporation of Ag. Further, Sr/Ag-containing TiO2 coatings with optimum Ag and Sr contents revealed good cytocompatibility, enhanced osteoblast spreading and osseointegration, which stemmed primarily from the synergistic effect exerted by the porous surface topography and the bioactive element Sr. However, this study has also identified, for the first time, that proper addition of Ag would further facilitate osteogenic effects. Besides, Sr may be able to alleviate the potential cytotoxic effect of excessive Ag. Thus, integration of optimum functional elements Ag and Sr into Ti-based implant materials would be expected to expedite osseointegration while simultaneously sustaining long-term antibacterial activity, which would provide new insights for relevant fundamental investigations and biomedical applications. PMID:27508428

  17. Tunable hydrophilicity on a hydrophobic fluorocarbon polymer coating on silicon

    SciTech Connect

    Kolari, K.; Hokkanen, A.

    2006-07-15

    An efficient, economic, reliable, and repeatable patterning procedure of hydrophobic surfaces was developed. A fluorocarbon polymer derived from the C{sub 4}F{sub 8} gas in an inductively coupled plasma etcher was used as the hydrophobic coating. For a subsequent patterning of hydrophilic apertures on the polymer, a short O{sub 2} plasma exposure through a silicon shadow mask was utilized. The overall hydrophilicity of the patterned surface can be tuned by the duration of the O{sub 2} plasma exposure, and also by the density and the size of the hydrophilic apertures. The laborious photolithography and tricky lift-off procedures are avoided. Optimization of the whole patterning process is explained thoroughly and supported with experimental data. The hydrophilic adhesion of the patterned polymer was evaluated with aqueous droplets, which were studied on matrices of the hydrophilic apertures of different sizes. The deposition parameters of the fluorocarbon polymer, the size of the droplet required to enable rolling on the patterned surface, and the duration of the O{sub 2} plasma exposure were considered as the main parameters. To determine the achievable resolution of the patterning procedure, the subsurface etching beneath the shadow mask was evaluated. The results show that a resolution of less than 10 {mu}m can be achieved. The simple hydrophilic patterning procedure described here can be used for the production of on-plane microfluidics, where a controlled adhesion or decohesion of 8-50 {mu}l droplets on the surface with a variable hydrophilicity from one location to another can be achieved.

  18. General Preparation of Three-Dimensional Porous Metal Oxide Foams Coated with Nitrogen-Doped Carbon for Enhanced Lithium Storage.

    PubMed

    Lu, Ke; Xu, Jiantie; Zhang, Jintao; Song, Bin; Ma, Houyi

    2016-07-13

    Porous metal oxide architectures coated with a thin layer of carbon are attractive materials for energy storage applications. Here, a series of porous metal oxide (e.g., vanadium oxides, molybdenum oxides, manganese oxides) foams with/without nitrogen-doped carbon (N-C) coating have been synthesized via a general surfactant-assisted template method, involving the formation of porous metal oxides coated with 1-hexadecylamine (HDA) and a subsequent thermal treatment. The presence of HDA is of importance for the formation of a porous structure, and the successive pyrolysis of such a nitrogen-containing surfactant generates nitrogen-doped carbon (N-C) coated on the surface of metal oxides, which also provides a facile way to adjust the valence states of metal oxides via the carbothermal reduction reaction. When used as electrode materials, the highly porous metal oxides with N-C coating exhibited enhanced performance for lithium ion storage, thanks to the unique 3D structures associated with highly porous structure and thin N-C coating. Typically, the porous metal oxides (V2O5, MoO3, MnO2) exhibited discharge capacities of 286, 303, and 463 mAh g(-1) at current densities of 30 and 100 mA g(-1), respectively. In contrast, the metal oxides with low valences and carbon coating (VO2@N-C, MoO2@N-C, and MnO@N-C) exhibited improved capacities of 461, 613, and 892 mAh g(-1). The capacity retentions of about 87.5, 80.2, and 85.0% for VO2@N-C, MoO2@N-C, and MnO@N-C were achieved after 600 cycles, suggesting the acceptable cycling stability. The present strategy would provide general guidance for preparing porous metal oxide foams with enhanced lithium storage performances. PMID:27322176

  19. Continuous preparation of polymer coated drug crystals by solid hollow fiber membrane-based cooling crystallization.

    PubMed

    Chen, Dengyue; Singh, Dhananjay; Sirkar, Kamalesh K; Pfeffer, Robert

    2016-02-29

    A facile way to continuously coat drug crystals with a polymer is needed in controlled drug release. Conventional polymer coating methods have disadvantages: high energy consumption, low productivity, batch processing. A novel method for continuous polymer coating of drug crystals based on solid hollow fiber cooling crystallization (SHFCC) is introduced here. The drug acting as the host particle and the polymer for coating are Griseofulvin (GF) and Eudragit RL100, respectively. The polymer's cloud point temperature in its acetone solution was determined by UV spectrophotometry. An acetone solution of the polymer containing the drug in solution as well as undissolved drug crystals in suspension were pumped through the tube side of the SHFCC device; a cold liquid was circulated in the shell side to rapidly cool down the feed solution-suspension in the hollow-fiber lumen. The polymer precipitated from the solution and coated the suspended crystals due to rapid temperature reduction and heterogeneous nucleation; crystals formed from the solution were also coated by the polymer. Characterizations by scanning electron microscopy, thermogravimetric analysis, laser diffraction spectroscopy, X-ray diffraction, Raman spectroscopy, and dissolution tests show that a uniformly coated, free-flowing drug/product can be obtained under appropriate operating conditions without losing the drug's pharmaceutical properties and controlled release characteristics. PMID:26772536

  20. Enhancement of Li+ ion conductivity in solid polymer electrolytes using surface tailored porous silica nanofillers

    NASA Astrophysics Data System (ADS)

    Mohanta, Jagdeep; Singh, Udai P.; Panda, Subhendu K.; Si, Satyabrata

    2016-09-01

    The current study represents the design and synthesis of polyethylene oxide (PEO)-based solid polymer electrolytes by solvent casting approach using surface tailored porous silica as nanofillers. The surface tailoring of porous silica nanostructure is achieved through silanization chemistry using 3-glycidyloxypropyl trimethoxysilane in which silane part get anchored to the silica surface whereas epoxy group get stellated from the silica surface. Surface tailoring of silica with epoxy group increases the room temperature electrochemical performances of the resulting polymer electrolytes. Ammonical hydrolysis of organosilicate precursor is used for both silica preparation and their surface tailoring. The composite solid polymer electrolyte films are prepared by solution mixing of PEO with lithium salt in presence of silica nanofillers and cast into film by solvent drying, which are then characterized by impedance measurement for conductivity study and wide angle x-ray diffraction for change in polymer crystallinity. Room temperature impedance measurement reveals Li+ ion conductivity in the order of 10‑4 S cm‑1, which is correlated to the decrease in PEO crystallinity. The enhancement of conductivity is further observed to be dependent on the amount of silica as well as on their surface characteristics.

  1. Ultra-Porous Nanoparticle Networks: A Biomimetic Coating Morphology for Enhanced Cellular Response and Infiltration

    PubMed Central

    Nasiri, Noushin; Ceramidas, Anthony; Mukherjee, Shayanti; Panneerselvan, Anitha; Nisbet, David R.; Tricoli, Antonio

    2016-01-01

    Orthopedic treatments are amongst the most common cause of surgery and are responsible for a large share of global healthcare expenditures. Engineering materials that can hasten bone integration will improve the quality of life of millions of patients per year and reduce associated medical costs. Here, we present a novel hierarchical biomimetic coating that mimics the inorganic constituent of mammalian bones with the aim of improving osseointegration of metallic implants. We exploit the thermally-driven self-organization of metastable core-shell nanoparticles during their aerosol self-assembly to rapidly fabricate robust, ultra-porous nanoparticle networks (UNN) of crystalline hydroxyapatite (HAp). Comparative analysis of the response of osteoblast cells to the ultra-porous nanostructured HAp surfaces and to the spin coated HAp surfaces revealed superior osseointegrative properties of the UNN coatings with significant cell and filopodia infiltration. This flexible synthesis approach for the engineering of UNN HAp coatings on titanium implants provides a platform technology to study the bone-implant interface for improved osseointegration and osteoconduction. PMID:27076035

  2. Processing Methods Established To Fabricate Porous Oxide Ceramic Spheres for Thermal Barrier Coating Applications

    NASA Technical Reports Server (NTRS)

    Dynys, Frederick W.

    2003-01-01

    As gas turbine technology advances, the demand for efficient engines and emission reduction requires a further increase in operating temperatures, but combustion temperatures are currently limited by the temperature capability of the engine components. The existing thermal barrier coating (TBC) technology does not provide sufficient thermal load reduction at a 3000 F (1649 C) operating condition. Advancement in thermal barrier coating technology is needed to meet this aggressive goal. One concept for improving thermal barrier coating effectiveness is to design coating systems that incorporate a layer that reflects or scatters photon radiation. This can be achieved by using porous structures. The refractive index mismatch between the solid and pore, the pore size, and the pore density can be engineered to efficiently scatter photon radiation. Under NASA s Ultra-Efficient Engine Technology (UEET) Program, processing methods to fabricate porous ceramic spheres suitable for scattering photon radiation at elevated temperatures have been established. A straightforward templating process was developed at the NASA Glenn Research Center that requires no special processing equipment. The template was used to define particle shape, particle size, and pore size. Spherical organic cation exchange resins were used as a structure-directing template. The cation exchange resins have dual template capabilities that can produce different pore architectures. This process can be used to fabricate both metal oxide and metal carbide spheres.

  3. Ultra-Porous Nanoparticle Networks: A Biomimetic Coating Morphology for Enhanced Cellular Response and Infiltration.

    PubMed

    Nasiri, Noushin; Ceramidas, Anthony; Mukherjee, Shayanti; Panneerselvan, Anitha; Nisbet, David R; Tricoli, Antonio

    2016-01-01

    Orthopedic treatments are amongst the most common cause of surgery and are responsible for a large share of global healthcare expenditures. Engineering materials that can hasten bone integration will improve the quality of life of millions of patients per year and reduce associated medical costs. Here, we present a novel hierarchical biomimetic coating that mimics the inorganic constituent of mammalian bones with the aim of improving osseointegration of metallic implants. We exploit the thermally-driven self-organization of metastable core-shell nanoparticles during their aerosol self-assembly to rapidly fabricate robust, ultra-porous nanoparticle networks (UNN) of crystalline hydroxyapatite (HAp). Comparative analysis of the response of osteoblast cells to the ultra-porous nanostructured HAp surfaces and to the spin coated HAp surfaces revealed superior osseointegrative properties of the UNN coatings with significant cell and filopodia infiltration. This flexible synthesis approach for the engineering of UNN HAp coatings on titanium implants provides a platform technology to study the bone-implant interface for improved osseointegration and osteoconduction. PMID:27076035

  4. Polymer degradation and molecular relaxation during accelerated weathering of coatings

    NASA Astrophysics Data System (ADS)

    Fernando, B. Malcolm Dilhan

    2011-12-01

    A model polyester-urethane coating similar to those on USAF aircraft was the focus in this research. It was studied for physical property changes during accelerated weathering. Isothermal aging and natural weathering were utilized as control studies. Coatings subjected to accelerated weathering had an increase in tensile modulus, glass transition temperature and surface stiffness. DSC analysis of these coatings clearly showed evidence for 'physical aging'. This phenomenon was pursued further to find out the impact of macromolecular relaxation on the polymer physical properties. The unique feature of this research is the investigation of kinetics of macromolecular relaxation whilst a polymer undergoes simultaneous degradation. Assessment was done for some material parameters as found in theoretical models. Fictive temperature (Tf), apparent activation energy (Deltah*/R) and non linearity parameter ( x) found in Tool-Narayanswamy-Moyniham (TNM) model were explored. Tf was found to be decreasing with weathering and explained the increasingly aged 'state' of the structure. Deltah*/R was found to be increasing and explains an increased energy barrier to overcome to attain relaxation. DSC peak-shift method was used to characterize x. At early stages there is a stronger non linearity of relaxation (lower x) with a stronger structure dependence and later the relaxation kinetics seems more temperature dependent (higher x). MDSC was done to characterize the non exponentiality parameter (beta) as found in the Kohlrauch-Williams-Watts (KWW) equation. Decreasing beta value with exposure implies an increasingly broad distribution of relaxation times. The Cooperatively Rearranging Regions (CRR) concept of Adams and Gibbs was also examined. Molecular weight (Ma) of the volume (Va) represented by a CRR was compared with Mc, the molecular weight between crosslinks. Nanoindentation was done to explore the coatings' surface mechanical properties. During accelerated weathering the

  5. Modified porous silica antireflective coatings with laser damage resistance for Ti:sapphire

    NASA Astrophysics Data System (ADS)

    Jia, Qiaoying; Li, Haiyuan; Liu, Ruijun; Tang, Yongxing; Jiang, Zhonghong

    2005-04-01

    Porous SiO2 antireflective (AR) coatings are prepared from the colloidal silica solution modified with methyltriethoxysilane (MTES) based on the sol-gel route. The viscosity of modified silica suspensions changes but their stability keeps when MTES is introduced. The refractive indices of modified coatings vary little after bake treatment from 100 to 150 Celsius. The modified silica coatings on Ti:sapphire crystal, owning good homogeneity, display prominent antireflective effect within the laser output waveband (750-850 nm) of Ti:sapphire lasers, with average transmission above 98.6%, and own laser induced damage thresholds (LIDTs) of more than 2.2 J/cm2 at 800 nm with the pulse duration of 300 ps.

  6. Simple push coating of polymer thin-film transistors.

    PubMed

    Ikawa, Mitsuhiro; Yamada, Toshikazu; Matsui, Hiroyuki; Minemawari, Hiromi; Tsutsumi, Jun'ya; Horii, Yoshinori; Chikamatsu, Masayuki; Azumi, Reiko; Kumai, Reiji; Hasegawa, Tatsuo

    2012-01-01

    Solution processibility is a unique advantage of organic semiconductors, permitting the low-cost production of flexible electronics under ambient conditions. However, the solution affinity to substrate surfaces remains a serious dilemma; liquid manipulation is more difficult on highly hydrophobic surfaces, but the use of such surfaces is indispensable for improving device characteristics. Here we demonstrate a simple technique, which we call 'push coating', to produce uniform large-area semiconducting polymer films over a hydrophobic surface with eliminating material loss. We utilize a poly(dimethylsiloxane)-based trilayer stamp whose conformal contact with the substrate enables capillarity-induced wetting of the surface. Films are formed through solvent sorption and retention in the stamp, allowing the stamp to be peeled perfectly from the film. The planar film formation on hydrophobic surfaces also enables subsequent fine film patterning. The technique improves the crystallinity and field-effect mobility of stamped semiconductor films, constituting a major step towards flexible electronics production. PMID:23132026

  7. Polymer Coated Echogenic Lipid Nanoparticles with Dual Release Triggers

    PubMed Central

    Nahire, Rahul; Haldar, Manas K.; Paul, Shirshendu; Mergoum, Anaas; Ambre, Avinash H.; Katti, Kalpana S.; Gange, Kara N.; Srivastava, D. K.; Sarkar, Kausik; Mallik, Sanku

    2013-01-01

    Although lipid nanoparticles are promising drug delivery vehicles, passive release of encapsulated contents at the target site is often slow. Herein, we report contents release from targeted, polymer coated, echogenic lipid nanoparticles in the cell cytoplasm by redox trigger and simultaneously enhanced by diagnostic frequency ultrasound. The lipid nanoparticles were polymerized on the external leaflet using a disulfide cross-linker. In the presence of cytosolic concentrations of glutathione, the lipid nanoparticles released 76% of encapsulated contents. Plasma concentrations of glutathione failed to release the encapsulated contents. Application of 3 MHz ultrasound for 2 minutes simultaneously with the reducing agent enhanced the release to 96%. Folic acid conjugated, doxorubicin loaded nanoparticles showed enhanced uptake and higher cytotoxicity in cancer cells overexpressing the folate receptor (compared to the control). With further developments, these lipid nanoparticles have the potential to be used as multimodal nanocarriers for simultaneous targeted drug delivery and ultrasound imaging. PMID:23394107

  8. Rapid removal of organic micropollutants from water by a porous β-cyclodextrin polymer

    NASA Astrophysics Data System (ADS)

    Alsbaiee, Alaaeddin; Smith, Brian J.; Xiao, Leilei; Ling, Yuhan; Helbling, Damian E.; Dichtel, William R.

    2016-01-01

    The global occurrence in water resources of organic micropollutants, such as pesticides and pharmaceuticals, has raised concerns about potential negative effects on aquatic ecosystems and human health. Activated carbons are the most widespread adsorbent materials used to remove organic pollutants from water but they have several deficiencies, including slow pollutant uptake (of the order of hours) and poor removal of many relatively hydrophilic micropollutants. Furthermore, regenerating spent activated carbon is energy intensive (requiring heating to 500-900 degrees Celsius) and does not fully restore performance. Insoluble polymers of β-cyclodextrin, an inexpensive, sustainably produced macrocycle of glucose, are likewise of interest for removing micropollutants from water by means of adsorption. β-cyclodextrin is known to encapsulate pollutants to form well-defined host-guest complexes, but until now cross-linked β-cyclodextrin polymers have had low surface areas and poor removal performance compared to conventional activated carbons. Here we crosslink β-cyclodextrin with rigid aromatic groups, providing a high-surface-area, mesoporous polymer of β-cyclodextrin. It rapidly sequesters a variety of organic micropollutants with adsorption rate constants 15 to 200 times greater than those of activated carbons and non-porous β-cyclodextrin adsorbent materials. In addition, the polymer can be regenerated several times using a mild washing procedure with no loss in performance. Finally, the polymer outperformed a leading activated carbon for the rapid removal of a complex mixture of organic micropollutants at environmentally relevant concentrations. These findings demonstrate the promise of porous cyclodextrin-based polymers for rapid, flow-through water treatment.

  9. Rapid removal of organic micropollutants from water by a porous β-cyclodextrin polymer.

    PubMed

    Alsbaiee, Alaaeddin; Smith, Brian J; Xiao, Leilei; Ling, Yuhan; Helbling, Damian E; Dichtel, William R

    2016-01-14

    The global occurrence in water resources of organic micropollutants, such as pesticides and pharmaceuticals, has raised concerns about potential negative effects on aquatic ecosystems and human health. Activated carbons are the most widespread adsorbent materials used to remove organic pollutants from water but they have several deficiencies, including slow pollutant uptake (of the order of hours) and poor removal of many relatively hydrophilic micropollutants. Furthermore, regenerating spent activated carbon is energy intensive (requiring heating to 500-900 degrees Celsius) and does not fully restore performance. Insoluble polymers of β-cyclodextrin, an inexpensive, sustainably produced macrocycle of glucose, are likewise of interest for removing micropollutants from water by means of adsorption. β-cyclodextrin is known to encapsulate pollutants to form well-defined host-guest complexes, but until now cross-linked β-cyclodextrin polymers have had low surface areas and poor removal performance compared to conventional activated carbons. Here we crosslink β-cyclodextrin with rigid aromatic groups, providing a high-surface-area, mesoporous polymer of β-cyclodextrin. It rapidly sequesters a variety of organic micropollutants with adsorption rate constants 15 to 200 times greater than those of activated carbons and non-porous β-cyclodextrin adsorbent materials. In addition, the polymer can be regenerated several times using a mild washing procedure with no loss in performance. Finally, the polymer outperformed a leading activated carbon for the rapid removal of a complex mixture of organic micropollutants at environmentally relevant concentrations. These findings demonstrate the promise of porous cyclodextrin-based polymers for rapid, flow-through water treatment. PMID:26689365

  10. Catalytic NO Oxidation in the Presence of Moisture Using Porous Polymers and Activated Carbon.

    PubMed

    Ghafari, Mohsen; Atkinson, John D

    2016-05-17

    NO oxidation catalyzed by porous materials is difficult to implement under industrial conditions because moisture in combustion exhaust streams blocks oxidation sites, decreasing NO conversion. In this work, hydrophobic cross-linked polymers are tested as NO oxidation catalysts to overcome these negative impacts associated with moisture. Although activated carbons (ACs) outperform hyper-cross-linked polymers by >88% and low-cross-linked polymers by >463% under dry conditions, their NO conversion drops to 0% when 50% relative humidity is added. Performance of hyper-cross-linked and low-cross-linked polymers, however, decreases by only 19-35% and <6%, respectively, for NO conversion in the presence of moisture. NO conversion differences between materials are attributed to differences in the catalysts' initial hydrophilicity and their proclivity to react with generated NO2, which also increases hydrophilicity. While the initial hydrophobicity of the polymers contributes to their consistent performance, it is their intrinsic ability to resist NO2 reduction reactions, compared to AC, that makes them the more viable catalyst for industrial application. Results suggest that the polymer hyper-cross-linking process improves steady-state NO conversion but increases NO2 surface reactivity and hydrophilicity. PMID:27075697

  11. Study on lotus-type porous copper electroplated with a Ni coating on inner surface of pores

    NASA Astrophysics Data System (ADS)

    Du, Hao; Song, Guihong; Nakajima, Hideo; Zhao, Yanhui; Xiao, Jinquan; Xiong, Tianying

    2013-01-01

    Deposition of Ni coating on inner surface of pores was attempted by electroplating for lotus-type porous copper with pore size of 0.6 mm and pore length of 6 mm. The surface morphology, thickness, thickness distribution along the pore length, and phase composition of the coating were characterized. It is proven that the Ni coating with a polycrystalline structure can be deposited on the inner surface of the pores with length/diameter of 10 for lotus-type porous copper by agitating the electroplating solution properly during the process. It is indicated that the coating thickness distributes uniformly along the pore depth and is about 4-5 μm. Furthermore, the mechanical properties including vicker hardness, compressive yield strength and absorbed energy ability of the electroplated porous copper were evaluated. It is found that the mechanical properties are improved significantly after depositing the nickel coating inside pores of the lotus-type porous copper. Among them, 0.2% yield stress increases from 22.96 to 30.15 MPa, while absorbed energy per volume from 60.83 to 96.01 MJ/m3 when compressed to strain of 80%, which is attributed mainly to the Ni coating as an obstacle to dislocation slip during deformation and its strengthening effect for the higher strength, and the good adhesion to the pore wall of the porous copper.

  12. Porous tantalum coatings prepared by vacuum plasma spraying enhance bmscs osteogenic differentiation and bone regeneration in vitro and in vivo.

    PubMed

    Tang, Ze; Xie, Youtao; Yang, Fei; Huang, Yan; Wang, Chuandong; Dai, Kerong; Zheng, Xuebin; Zhang, Xiaoling

    2013-01-01

    Tantalum, as a potential metallic implant biomaterial, is attracting more and more attention because of its excellent anticorrosion and biocompatibility. However, its significantly high elastic modulus and large mechanical incompatibility with bone tissue make it unsuitable for load-bearing implants. In this study, porous tantalum coatings were first successfully fabricated on titanium substrates by vacuum plasma spraying (VPS), which would exert the excellent biocompatibility of tantalum and alleviate the elastic modulus of tantalum for bone tissue. We evaluated cytocompatibility and osteogenesis activity of the porous tantalum coatings using human bone marrow stromal cells (hBMSCs) and its ability to repair rabbit femur bone defects. The morphology and actin cytoskeletons of hBMSCs were observed via electron microscopy and confocal, and the cell viability, proliferation and osteogenic differentiation potential of hBMSCs were examined quantitatively by PrestoBlue assay, Ki67 immunofluorescence assay, real-time PCR technology and ALP staining. For in vivo detection, the repaired femur were evaluated by histomorphology and double fluorescence labeling 3 months postoperation. Porous tantalum coating surfaces promoted hBMSCs adhesion, proliferation, osteogenesis activity and had better osseointegration and faster new bone formation rate than titanium coating control. Our observation suggested that the porous tantalum coatings had good biocompatibility and could enhance osseoinductivity in vitro and promote new bone formation in vivo. The porous tantalum coatings prepared by VPS is a promising strategy for bone regeneration. PMID:23776648

  13. Porous Tantalum Coatings Prepared by Vacuum Plasma Spraying Enhance BMSCs Osteogenic Differentiation and Bone Regeneration In Vitro and In Vivo

    PubMed Central

    Tang, Ze; Xie, Youtao; Yang, Fei; Huang, Yan; Wang, Chuandong; Dai, Kerong; Zheng, Xuebin; Zhang, Xiaoling

    2013-01-01

    Tantalum, as a potential metallic implant biomaterial, is attracting more and more attention because of its excellent anticorrosion and biocompatibility. However, its significantly high elastic modulus and large mechanical incompatibility with bone tissue make it unsuitable for load-bearing implants. In this study, porous tantalum coatings were first successfully fabricated on titanium substrates by vacuum plasma spraying (VPS), which would exert the excellent biocompatibility of tantalum and alleviate the elastic modulus of tantalum for bone tissue. We evaluated cytocompatibility and osteogenesis activity of the porous tantalum coatings using human bone marrow stromal cells (hBMSCs) and its ability to repair rabbit femur bone defects. The morphology and actin cytoskeletons of hBMSCs were observed via electron microscopy and confocal, and the cell viability, proliferation and osteogenic differentiation potential of hBMSCs were examined quantitatively by PrestoBlue assay, Ki67 immunofluorescence assay, real-time PCR technology and ALP staining. For in vivo detection, the repaired femur were evaluated by histomorphology and double fluorescence labeling 3 months postoperation. Porous tantalum coating surfaces promoted hBMSCs adhesion, proliferation, osteogenesis activity and had better osseointegration and faster new bone formation rate than titanium coating control. Our observation suggested that the porous tantalum coatings had good biocompatibility and could enhance osseoinductivity in vitro and promote new bone formation in vivo. The porous tantalum coatings prepared by VPS is a promising strategy for bone regeneration. PMID:23776648

  14. Influence of implantation on the electrochemical properties of smooth and porous TiN coatings for stimulation electrodes

    NASA Astrophysics Data System (ADS)

    Meijs, S.; Sørensen, C.; Sørensen, S.; Rechendorff, K.; Fjorback, M.; Rijkhoff, N. J. M.

    2016-04-01

    Objective. To determine whether changes in electrochemical properties of porous titanium nitride (TiN) electrodes as a function of time after implantation are different from those of smooth TiN electrodes. Approach. Eight smooth and 8 porous TiN coated electrodes were implanted in 8 rats. Before implantation, voltage transients, cyclic voltammograms and impedance spectra were recorded in phosphate buffered saline (PBS). After implantation, these measurements were done weekly to investigate how smooth and porous electrodes were affected by implantation. Main results. The electrode capacitance of the porous TiN electrodes decreased more than the capacitance of the smooth electrodes due to acute implantation under fast measurement conditions (such as stimulation pulses). This indicates that protein adhesion presents a greater diffusion limitation for counter-ions for the porous than for the smooth electrodes. The changes in electrochemical properties during the implanted period were similar for smooth and porous TiN electrodes, indicating that cell adhesion poses a similar diffusion limitation for smooth and porous electrodes. Significance. This knowledge can be used to optimize the porous structure of the TiN film, so that the effect of protein adhesion on the electrochemical properties is diminished. Alternatively, an additional coating could be applied on the porous TiN that would prevent or minimize protein adhesion.

  15. Fabrication of Optical Multilayer Devices from Porous Silicon Coatings with Closed Porosity by Magnetron Sputtering.

    PubMed

    Caballero-Hernández, Jaime; Godinho, Vanda; Lacroix, Bertrand; Jiménez de Haro, Maria C; Jamon, Damien; Fernández, Asunción

    2015-07-01

    The fabrication of single-material photonic-multilayer devices is explored using a new methodology to produce porous silicon layers by magnetron sputtering. Our bottom-up methodology produces highly stable amorphous porous silicon films with a controlled refractive index using magnetron sputtering and incorporating a large amount of deposition gas inside the closed pores. The influence of the substrate bias on the formation of the closed porosity was explored here for the first time when He was used as the deposition gas. We successfully simulated, designed, and characterized Bragg reflectors and an optical microcavity that integrates these porous layers. The sharp interfaces between the dense and porous layers combined with the adequate control of the refractive index and thickness allowed for excellent agreement between the simulation and the experiments. The versatility of the magnetron sputtering technique allowed for the preparation of these structures for a wide range of substrates such as polymers while also taking advantage of the oblique angle deposition to prepare Bragg reflectors with a controlled lateral gradient in the stop band wavelengths. PMID:26046812

  16. Polymer composites and porous materials prepared by thermally induced phase separation and polymer-metal hybrid methods

    NASA Astrophysics Data System (ADS)

    Yoon, Joonsung

    The primary objective of this research is to investigate the morphological and mechanical properties of composite materials and porous materials prepared by thermally induced phase separation. High melting crystallizable diluents were mixed with polymers so that the phase separation would be induced by the solidification of the diluents upon cooling. Theoretical phase diagrams were calculated using Flory-Huggins solution thermodynamics which show good agreement with the experimental results. Porous materials were prepared by the extraction of the crystallized diluents after cooling the mixtures (hexamethylbenzene/polyethylene and pyrene/polyethylene). Anisotropic structures show strong dependence on the identity of the diluents and the composition of the mixtures. Anisotropic crystal growth of the diluents was studied in terms of thermodynamics and kinetics using DSC, optical microscopy and SEM. Microstructures of the porous materials were explained in terms of supercooling and dendritic solidification. Dual functionality of the crystallizable diluents for composite materials was evaluated using isotactic polypropylene (iPP) and compatible diluents that crystallize upon cooling. The selected diluents form homogeneous mixtures with iPP at high temperature and lower the viscosity (improved processability), which undergo phase separation upon cooling to form solid particles that function as a toughening agent at room temperature. Tensile properties and morphology of the composites showed that organic crystalline particles have the similar effect as rigid particles to increase toughness; de-wetting between the particle and iPP matrix occurs at the early stage of deformation, followed by unhindered plastic flow that consumes significant amount of fracture energy. The effect of the diluents, however, strongly depends on the identity of the diluents that interact with the iPP during solidification step, which was demonstrated by comparing tetrabromobisphenol-A and

  17. Three-dimensional conformal coatings through the entrapment of polymer membrane precursors.

    PubMed

    Nguyen, Du T; Kleiman, Maya; Ryu, Keun Ah; Hiew, Stanley; Brubaker, Kyle; Mughnetsyan, Rafik; Truong, Richard; Dolan, Benjamin; Tackett, Edward; Esser-Kahn, Aaron P

    2014-02-26

    We report a technique to coat polymers onto 3D surfaces distinct from traditional spray, spin, or dip coating. In our technique, the surface of a template structure composed of poly(lactic acid) swells and entraps a soluble polymer precursor. Once entrapped, the precursor is cured, resulting in a thin, conformal membrane. The thickness of each coating depends on the coating solution composition, residence time, and template size. Thicknesses ranged from 400 nm to 4 μm within the experimental conditions we explored. The coating method was compatible with a range of polymers. Complicated 3D structures and microstructures of 10 μm thickness and separation were coated using this technique. The templates can also be selectively removed, leaving behind a hollow membrane structure in the shape of the original printed, extruded, or microporous template structures. This technique may be useful in applications that benefit from three-dimensional membrane topologies, including catalysis, separations, and potentially tissue engineering. PMID:24437474

  18. Enhanced ionic polymer metal composite actuator with porous nafion membrane using zinc oxide particulate leaching method

    NASA Astrophysics Data System (ADS)

    Jung, Sun Yong; Ko, Seong Young; Park, Jong-Oh; Park, Sukho

    2015-03-01

    In this study, to improve the performance of an ionic polymer metal composite (IPMC), we suggest a porous nafion membrane fabricated with the particulate leaching method with zinc oxide and propose an IPMC that uses the porous nafion membrane. To fabricate this membrane, the proper ratio of nafion and zinc oxide powder is dispersed in a solvent. Then the zinc oxide embedded in the nafion membrane is fabricated with a casting method. With the particulate leaching method, the embedded zinc oxide particles are dissolved by an acid solution, and the spaces of the zinc oxide particles changed to pores. Finally, through electroless plating and ion exchange procedures, an IPMC with the porous nafion membrane is fabricated. The proposed IPMC has higher water uptake (WUP) and ion exchange capacity (IEC) and can show better actuation performance compared to the conventional nafion-based IPMC. We also measure the actuation displacement and blocking forces of the proposed IPMC. Compared with the conventional nafion-based IPMC, the proposed IPMC with the porous nafion membrane has increased displacements: about 80% at ac input and about 250% at dc input, and increased blocking force about 130% at dc input.

  19. Coating of meso-porous metallic membranes with oriented channel-likefine pores by pulsed laser deposition

    NASA Astrophysics Data System (ADS)

    Mukherji, D.; Lackner, J.; Wanderka, N.; Kardjilov, N.; Näth, O.; Jäger, S.; Schmitz, F.; Rösler, J.

    2008-02-01

    There is increasing demand to functionalize meso- and nanoporous materials by coating and make the porous substrate biocompatible or environmentally friendly. However, coating on a meso-porous substrate poses great challenges, especially if the pore aspect ratio is high. We adopted the pulsed laser deposition (PLD) method to coat Ni3Al-based meso-porous membranes, which were fabricated from a single-crystal Ni-based superalloy by a unique selective phase dissolution technique. These membranes were about 250 µm thick and had channel-like pores (~200 nm wide) with very high aspect ratio. Two different coating materials, i.e. diamond-like carbon (DLC) and titanium, were used to coat these membranes. High energy C or Ti ions, produced in the plasma plume by the PLD process, penetrated the channel-like pores and deposited coatings on the pore walls deep inside the membrane. The thickness and the quality of coatings on the pore walls were examined using the dual-beam system. The coating thickness, of the order of 50 nm, was adherent to the pore walls and was quite uniform at different depths. The carbon and the Ti deposition behaved quite similarly. The preliminary experiments showed that the PLD is an adequate method for coating fine open cavities of complex geometry. Simulations based on stopping and the range of ions in matter (SRIM) calculations helped in understanding the deposition processes on pore walls at great depths.

  20. Data on bone marrow stem cells delivery using porous polymer scaffold

    PubMed Central

    Geesala, Ramasatyaveni; Bar, Nimai; Dhoke, Neha R.; Basak, Pratyay; Das, Amitava

    2015-01-01

    Low bioavailability and/or survival at the injury site of transplanted stem cells necessitate its delivery using a biocompatible, biodegradable cell delivery vehicle. In this dataset, we report the application of a porous biocompatible, biodegradable polymer network that successfully delivers bone marrow stem cells (BMSCs) at the wound site of a murine excisional splint wound model. In this data article, we are providing the additional data of the reference article “Porous polymer scaffold for on-site delivery of stem cells – protects from oxidative stress and potentiates wound tissue repair” (Ramasatyaveni et al., 2016) [1]. This data consists of the characterization of bone marrow stem cells (BMSCs) showing the pluripotency and stem cell-specific surface markers. Image analysis of the cellular penetration into PEG–PU polymer network and the mechanism via enzymatic activation of MMP-2 and MMP-13 are reported. In addition, we provide a comparison of various routes of transplantation-mediated BMSCs engraftment in the murine model using bone marrow transplantation chimeras. Furthermore, we included in this dataset the engraftment of BMSCs expressing Sca-1+Lin−CD133+CD90.2+ in post-surgery day 10. PMID:26862563

  1. A novel surface modification technique for forming porous polymer monoliths in poly(dimethylsiloxane)

    PubMed Central

    Burke, Jeffrey M.; Smela, Elisabeth

    2012-01-01

    A new method of surface modification is described for enabling the in situ formation of homogenous porous polymer monoliths (PPMs) within poly(dimethylsiloxane) (PDMS) microfluidic channels that uses 365 nm UV illumination for polymerization. Porous polymer monolith formation in PDMS can be challenging because PDMS readily absorbs the monomers and solvents, changing the final monolith morphology, and because PDMS absorbs oxygen, which inhibits free-radical polymerization. The new approach is based on sequentially absorbing a non-hydrogen-abstracting photoinitiator and the monomers methyl methacrylate and ethylene diacrylate within the walls of the microchannel, and then polymerizing the surface treatment polymer within the PDMS, entangled with it but not covalently bound. Four different monolith compositions were tested, all of which yielded monoliths that were securely anchored and could withstand pressures exceeding the bonding strength of PDMS (40 psi) without dislodging. One was a recipe that was optimized to give a larger average pore size, required for low back pressure. This monolith was used to concentrate and subsequently mechanical lyse B lymphocytes. PMID:22685511

  2. Polyaniline-coated freestanding porous carbon nanofibers as efficient hybrid electrodes for supercapacitors

    NASA Astrophysics Data System (ADS)

    Tran, Chau; Singhal, Richa; Lawrence, Daniel; Kalra, Vibha

    2015-10-01

    Three-dimensional, free-standing, hybrid supercapacitor electrodes combining polyaniline (PANI) and porous carbon nanofibers (P-CNFs) were fabricated with the aim to integrate the benefits of both electric double layer capacitors (high power, cyclability) and pseudocapacitors (high energy density). A systematic investigation of three different electropolymerization techniques, namely, potentiodynamic, potentiostatic, and galvanostatic, for electrodeposition of PANI on freestanding carbon nanofiber mats was conducted. It was found that the galvanostatic method, where the current density is kept constant and can be easily controlled facilitates conformal and uniform coating of PANI on three-dimensional carbon nanofiber substrates. The electrochemical tests indicated that the PANI-coated P-CNFs exhibit excellent specific capacitance of 366 F g-1 (vs. 140 F g-1 for uncoated porous carbon nanofibers), 140 F cm-3 volumetric capacitance, and up to 2.3 F cm-2 areal capacitance at 100 mV s-1 scan rate. Such excellent performance is attributed to a thin and conformal coating of PANI achieved using the galvanostatic electrodeposition technique, which not only provides pseudocapacitance with high rate capability, but also retains the double-layer capacitance of the underlying P-CNFs.

  3. Initial evaluation of bone ingrowth into a novel porous titanium coating.

    PubMed

    Wazen, Rima M; Lefebvre, Louis-Philippe; Baril, Eric; Nanci, Antonio

    2010-07-01

    Porous metals (sintered beads and meshes) have been used for many years for different orthopedic applications. Metal foams have been recently developed. These foams have the advantage of being more porous than the traditional coatings. Their high porosity provides more space for bone ingrowth and mechanical interlocking and presents more surface for implant-bone contact. The objective of this study was to evaluate in vivo bone ingrowth into Ti implants covered with a novel Ti foam coating. This foam contains 50% in volume of interconnected pores and a higher surface area compared to dense Ti. Both coated implants and dense Ti controls were placed transcortically in the rat tibia. The animals were sacrificed at 2 weeks after implantation, and the amount of bone in the implants was determined using backscattered electron imaging and X-ray microtomography. Already at this time interval, the pores within the Ti foam showed 97.7% bone filling, and the bone-implant contact area was significantly increased compared to dense Ti controls. These initial results indicate that this novel Ti foam is biocompatible, has the capacity to sustain bone formation, and can potentially improve osseointegration. PMID:20336725

  4. Utilization of star-shaped polymer architecture in the creation of high-density polymer brush coatings for the prevention of platelet and bacteria adhesion

    PubMed Central

    Totani, Masayasu; Terada, Kayo; Terashima, Takaya; Kim, Ill Yong; Ohtsuki, Chikara; Xi, Chuanwu; Tanihara, Masao

    2014-01-01

    We demonstrate utilization of star-shaped polymers as high-density polymer brush coatings and their effectiveness to inhibit the adhesion of platelets and bacteria. Star polymers consisting of poly(2-hydroxyethyl methacrylate) (PHEMA) and/or poly(methyl methacrylate) (PMMA), were synthesized using living radical polymerization with a ruthenium catalyst. The polymer coatings were prepared by simple drop casting of the polymer solution onto poly(ethylene terephthalate) (PET) surfaces and then dried. Among the star polymers prepared in this study, the PHEMA star polymer (star-PHEMA) and the PHEMA/PMMA (mol. ratio of 71/29) heteroarm star polymer (star-H71M29) coatings showed the highest percentage of inhibition against platelet adhesion (78–88% relative to noncoated PET surface) and Escherichia coli (94–97%). These coatings also showed anti-adhesion activity against platelets after incubation in Dulbecco's phosphate buffered saline or surfactant solution for 7 days. In addition, the PMMA component of the star polymers increased the scratch resistance of the coating. These results indicate that the star-polymer architecture provides high polymer chain density on PET surfaces to prevent adhesion of platelets and bacteria, as well as coating stability and physical durability to prevent exposure of bare PET surfaces. The star polymers provide a simple and effective approach to preparing anti-adhesion polymer coatings on biomedical materials against the adhesion of platelets and bacteria. PMID:25485105

  5. Utilization of star-shaped polymer architecture in the creation of high-density polymer brush coatings for the prevention of platelet and bacteria adhesion.

    PubMed

    Totani, Masayasu; Ando, Tsuyoshi; Terada, Kayo; Terashima, Takaya; Kim, Ill Yong; Ohtsuki, Chikara; Xi, Chuanwu; Kuroda, Kenichi; Tanihara, Masao

    2014-09-01

    We demonstrate utilization of star-shaped polymers as high-density polymer brush coatings and their effectiveness to inhibit the adhesion of platelets and bacteria. Star polymers consisting of poly(2-hydroxyethyl methacrylate) (PHEMA) and/or poly(methyl methacrylate) (PMMA), were synthesized using living radical polymerization with a ruthenium catalyst. The polymer coatings were prepared by simple drop casting of the polymer solution onto poly(ethylene terephthalate) (PET) surfaces and then dried. Among the star polymers prepared in this study, the PHEMA star polymer (star-PHEMA) and the PHEMA/PMMA (mol. ratio of 71/29) heteroarm star polymer (star-H71M29) coatings showed the highest percentage of inhibition against platelet adhesion (78-88% relative to noncoated PET surface) and Escherichia coli (94-97%). These coatings also showed anti-adhesion activity against platelets after incubation in Dulbecco's phosphate buffered saline or surfactant solution for 7 days. In addition, the PMMA component of the star polymers increased the scratch resistance of the coating. These results indicate that the star-polymer architecture provides high polymer chain density on PET surfaces to prevent adhesion of platelets and bacteria, as well as coating stability and physical durability to prevent exposure of bare PET surfaces. The star polymers provide a simple and effective approach to preparing anti-adhesion polymer coatings on biomedical materials against the adhesion of platelets and bacteria. PMID:25485105

  6. Synthetic Methodology for the Fabrication of Porous Porphyrin Materials with Metal-Organic-Polymer Aerogels.

    PubMed

    Zhao, Xin; Yuan, Lin; Zhang, Zeng-Qi; Wang, Yong-Song; Yu, Qiong; Li, Jun

    2016-06-01

    A promising fabrication strategy used for designing porous porphyrin materials and a group of rigid carboxyl porphyrins based metal-organic-polymer aerogels (MOPAs) has been proposed recently. These newly synthesized MOPAs were exemplarily characterized by FT-IR, UV-vis-DRS, EDS, PXRD, TGA, SEM, TEM, and gas sorption measurements. A gelation study has shown that solvents, molar ratio, temperature, and peripheral carboxyl number in porphyrins all affect gel generation. The MOPA series exhibit eminent thermal stability, high removal efficiency in dye adsorption, versatile morphologies, and permanent tunable porosity; also the BET surface areas fall within the range 249-779 m(2) g(-1). All of the mentioned properties are significantly superior to some other porous materials, which enable these compounds to be potential candidates for dye uptake, gas storage, and separation. PMID:27159626

  7. Novel thiophene-bearing conjugated microporous polymer honeycomb-like porous spheres with ultrahigh iodine uptake.

    PubMed

    Ren, Feng; Zhu, Zhaoqi; Qian, Xin; Liang, Weidong; Mu, Peng; Sun, Hanxue; Liu, Jiehua; Li, An

    2016-07-28

    Two conjugated microporous polymers containing thiophene-moieties (SCMPs) were obtained by the polymerization of 3,3',5,5'-tetrabromo-2,2'-bithiophene and ethynylbenzene monomers through the palladium-catalyzed Sonogashira-Hagihara crosscoupling reaction. The resulting SCMPs show high thermal stability with a decomposition temperature above 300 °C. Scanning electron microscopy images show that the resulting SCMPs formed as an aggregation composed of micrometer-sized SCMP spheres, in which honeycomb-like porous spheres with penetrated pores on the surface were observed. Taking advantage of such a unique honeycomb-like porous morphology as well as π-conjugated structures, the SCMPs show ultrahigh absorption performance for iodine vapour with an uptake of up to 345 wt% obtained, which is the highest value reported to date for CMPs, thus making the resulting SCMPs ideal absorbent materials for reversible iodine capture to address environmental issues. PMID:27417941

  8. Effects of Calcination Condition on Porous Reduced Titanium Oxides and Oxynitrides via Preceramic Polymer Route

    SciTech Connect

    Hasegawa, George; Sato, Tatsuya; Kanamori, Kazuyoshi; Sun, Cheng-Jun; Ren, Yang; Kobayashi, Yoji; Kageyama, Hiroshi; Abe, Takeshi; Nakanishi, Kazuki

    2015-03-16

    The preceramic polymer route from titanium-based inorganic-organic hybrid networks provides electro conductive N-doped reduced titanium oxides (TinO2n–1) and titanium oxynitrides (TiOxNy) with a monolithic shape as well as well-defined porous structure. This methodology demonstrates advantageously lower temperature of crystal phase transition compared to the reduction of TiO2 by carbon or H2. In this study, effects of calcination condition on various features of the products have been explored by adopting three different atmospheric conditions and varying the calcination temperature. The detailed crystallographic and elemental analyses disclose the distinguished difference in phase transition behavior with respect to calcination atmosphere. Correlation between the crystallization and nitridation behaviors, porous properties and electric conductivities in the final products has been discussed.

  9. Strengthening of polymer ordered porous materials based on a layered nanocomposite internal structure.

    PubMed

    Heng, Liping; Guo, Xieyou; Guo, Tianqi; Wang, Bin; Jiang, Lei

    2016-07-21

    Ordered porous polymeric films attract more and more attention because they have many advantages and broad application prospects in many fields. But because of their large flexibility and poor mechanical properties, some of the scope for application is greatly limited. Inspired by the ordered pore structure of the honeycomb and the layered structure of natural nacre, we prepared an ordered porous polymer film with a layered structure in the pore wall by the solvent-evaporation-restriction assisted hard template method. Compared with other samples, this kind of film with the layered structure showed both excellent mechanical properties and good stability. This kind of film with high mechanical strength, is considered to have wide applications in the areas of separation, biomedicine, precision instruments, aerospace, environmental protection and so on. PMID:27355160

  10. A Dry Powder Process for Preparing Uni-Tape Prepreg from Polymer Powder Coated Filamentary Towpregs

    NASA Technical Reports Server (NTRS)

    Wilkinson, Steven P. (Inventor); Johnston, Norman J. (Inventor); Marchello, Joseph M. (Inventor)

    1995-01-01

    A process for preparing uni-tape prepreg from polymer powder coated filamentary towpregs is provided. A plurality of polymer powder coated filamentary towpregs are provided. The towpregs are collimated so that each towpreg is parallel. The sandwich is heated to a temperature wherein the polymer flows and intimately contacts the filaments and pressure is repeatedly applied perpendicularly to the sandwich with a longitudinal oscillating action wherein the filaments move apart and the polymer wets the filaments forming a uni-tape prepreg. The uni-tape prepreg is subsequently cooled.

  11. Dry powder process for preparing uni-tape prepreg from polymer powder coated filamentary towpregs

    NASA Technical Reports Server (NTRS)

    Wilkinson, Steven P. (Inventor); Johnston, Norman J. (Inventor); Marchello, Joseph M. (Inventor)

    1997-01-01

    A process for preparing uni-tape prepreg from polymer powder coated filamentary towpregs is provided. A plurality of polymer powder coated filamentary towpregs are provided. The towpregs are collimated so that each towpreg is parallel. A material is applied to each side of the towpreg to form a sandwich. The sandwich is heated to a temperature wherein the polymer flows and intimately contacts the filaments and pressure is repeatedly applied perpendicularly to the sandwich with a longitudinal oscillating action wherein the filaments move apart and the polymer wets the filaments forming a uni-tape prepreg. The uni-tape prepreg is subsequently cooled.

  12. Strengthening of polymer ordered porous materials based on a layered nanocomposite internal structure

    NASA Astrophysics Data System (ADS)

    Heng, Liping; Guo, Xieyou; Guo, Tianqi; Wang, Bin; Jiang, Lei

    2016-07-01

    Ordered porous polymeric films attract more and more attention because they have many advantages and broad application prospects in many fields. But because of their large flexibility and poor mechanical properties, some of the scope for application is greatly limited. Inspired by the ordered pore structure of the honeycomb and the layered structure of natural nacre, we prepared an ordered porous polymer film with a layered structure in the pore wall by the solvent-evaporation-restriction assisted hard template method. Compared with other samples, this kind of film with the layered structure showed both excellent mechanical properties and good stability. This kind of film with high mechanical strength, is considered to have wide applications in the areas of separation, biomedicine, precision instruments, aerospace, environmental protection and so on.Ordered porous polymeric films attract more and more attention because they have many advantages and broad application prospects in many fields. But because of their large flexibility and poor mechanical properties, some of the scope for application is greatly limited. Inspired by the ordered pore structure of the honeycomb and the layered structure of natural nacre, we prepared an ordered porous polymer film with a layered structure in the pore wall by the solvent-evaporation-restriction assisted hard template method. Compared with other samples, this kind of film with the layered structure showed both excellent mechanical properties and good stability. This kind of film with high mechanical strength, is considered to have wide applications in the areas of separation, biomedicine, precision instruments, aerospace, environmental protection and so on. Electronic supplementary information (ESI) available: SEM image of hexagonal silicon pillar templates, AFM images of clay platelets on a silicon substrate, photographs of free-standing gels, X-ray diffraction profiles for dried materials, FTIR and TGA of the samples, and

  13. High internal phase emulsion with double emulsion morphology and their templated porous polymer systems.

    PubMed

    Lei, Lei; Zhang, Qi; Shi, Shuxian; Zhu, Shiping

    2016-12-01

    This paper reports synthesis of the first high internal phase emulsion (HIPE) system with double emulsion (DE) morphology (HIPE-DE). HIPE is a highly concentrated but highly stable emulsion system, which has a dispersed/internal phase fraction over 74vol%. DE represents an emulsion system that hierarchically encapsulates two immiscible phases. The combination of HIPE and DE provides an efficient method for fabrication of complex structures. In this work, HIPE-DE having a water-in-oil-in-water (W/O/W) morphology has been prepared for the first time via a simple one-step emulsification method with poly(2-(diethylamino)ethyl methacrylate) (PDEA) microgel particles as Pickering stabilizer. An oil phase fraction up to 90vol% was achieved by optimizing the microgel concentration in aqueous phase. The mechanism of the DE formation has been elucidated. It was found that while PDEA microgels stabilized the oil droplets in water, small amount protonated DEA monomers acted as surfactant and formed water-containing micelles inside the oil droplets. It was demonstrated that the W/O/W HIPE-DE could be precisely converted into porous polymer structures. With styrene as the oil phase in W/O/W HIPE-DE, porous polystyrene particles were obtained upon polymerization. With dissolved acrylamide as the aqueous phase and toluene as the continuous phase, porous polyacrylamide matrixes were prepared. Elevating temperature required for polymerization did not change the W/O/W HIPE-DE morphologies. This simple approach provides a versatile platform for synthesis of a variety of porous polymer systems. PMID:27560496

  14. Novel mucoadhesion tests for polymers and polymer-coated particles to design optimal mucoadhesive drug delivery systems.

    PubMed

    Takeuchi, Hirofumi; Thongborisute, Jringjai; Matsui, Yuji; Sugihara, Hikaru; Yamamoto, Hiromitsu; Kawashima, Yoshiaki

    2005-11-01

    To design an effective particulate drug delivery system having mucoadhesive function, several mucoadhesion tests for polymers and the resultant particulate systems were developed. Mucin particle method is a simple mucoadhesion test for polymers, in which the commercial mucin particles are used. By measuring the change in particle size or zeta potential of the mucin particle in a certain concentration of polymer solution, we could estimate the extent of their mucoadhesive property. BIACORE method is also a novel mucoadhesion test for polymers. On passing through the mucin suspension on the polymer-immobilized chip of BIACORE instrument, the interaction was quantitatively evaluated with the change in its response diagram. By using these mucoadhesion tests, we detected a strong mucoadhesive property of several types of chitosan and Carbopol. Evaluation of mucoadhesive property of polymer-coated particulate systems was demonstrated with the particle counting method developed by us. To detect the mucoadhesive phenomena in the intestinal tract, we observed the rat intestine with the confocal laser scanning microscope (CLSM) after oral administration of the particulate systems. The resultant photographs clearly showed a longer retention of submicron-sized chitosan-coated liposomes (ssCS-Lip) in the intestinal tract than other liposomal particles tested such as non-coated liposomes and chitosan-coated multilamellar one. These observations explained well the superiority of the ssCS-Lip as drug carrier in oral administration of calcitonin in rats than other liposomal particles. PMID:16169120

  15. Controllable growth of porous structures from co-continuous polymer blend

    NASA Astrophysics Data System (ADS)

    Zhang, Wei

    To enable controllable generation of porous structures, a set of new fabrication techniques utilizing the annealing kinetics of co-continuous polymer blends were proposed and investigated. As the first step towards the creation of an organized porous material, a new technique based on regulating the thermal boundary conditions to controllably grow gradient porous structures was developed. In this technique, specially designed thermal boundaries were used to generate a well-defined temperature field inside a co-continuous polymer blend with fine phase structure. Because of the temperature dependency of zero-shear viscosity and its influence on phase coarsening rate, a graded phase size distribution was generated by this temperature field. After one component was selectively dissolved, a gradient porous structure was produced. To demonstrate the versatility of this technique, three different gradient porous structures were created. After the effectiveness of thermal boundary condition in developing organized porous materials was verified, the possibility of utilizing kinematic and dynamic boundary conditions to obtain extra controllability was investigated. Two types of kinematic boundary conditions, no-slip wall and 1D hard wall confinement were tested separately. It was found that no-slip wall could greatly slow down the phase coarsening rate of the nearby polymer blend. When a no-slip wall and a fully slip wall were applied at each side of a molten co-continuous blend, a pore size gradient was generated in the direction perpendicular to the wall surface with smaller pores near the no-slip wall. One directional hard wall confinement formed by a pair of fully slip parallel walls led to the formation of an aligned phase structure oriented in the vertical direction to the walls. Experiments regarding the effect of dynamic boundary condition were conducted by imposing different chemical potentials at the surface of molten blend. Fully dense surface and completely open

  16. Process to produce lithium-polymer batteries

    DOEpatents

    MacFadden, Kenneth Orville

    1998-01-01

    A polymer bonded sheet product suitable for use as an electrode in a non-aqueous battery system. A porous electrode sheet is impregnated with a solid polymer electrolyte, so as to diffuse into the pores of the electrode. The composite is allowed to cool, and the electrolyte is entrapped in the porous electrode. The sheet products composed have the solid polymer electrolyte composition diffused into the active electrode material by melt-application of the solid polymer electrolyte composition into the porous electrode material sheet. The solid polymer electrolyte is maintained at a temperature that allows for rapid diffusion into the pores of the electrode. The composite electrolyte-electrode sheets are formed on current collectors and can be coated with solid polymer electrolyte prior to battery assembly. The interface between the solid polymer electrolyte composite electrodes and the solid polymer electrolyte coating has low resistance.

  17. Process to produce lithium-polymer batteries

    DOEpatents

    MacFadden, K.O.

    1998-06-30

    A polymer bonded sheet product is described suitable for use as an electrode in a non-aqueous battery system. A porous electrode sheet is impregnated with a solid polymer electrolyte, so as to diffuse into the pores of the electrode. The composite is allowed to cool, and the electrolyte is entrapped in the porous electrode. The sheet products composed have the solid polymer electrolyte composition diffused into the active electrode material by melt-application of the solid polymer electrolyte composition into the porous electrode material sheet. The solid polymer electrolyte is maintained at a temperature that allows for rapid diffusion into the pores of the electrode. The composite electrolyte-electrode sheets are formed on current collectors and can be coated with solid polymer electrolyte prior to battery assembly. The interface between the solid polymer electrolyte composite electrodes and the solid polymer electrolyte coating has low resistance. 1 fig.

  18. Selective Adsorption of CO2 from Light Gas Mixtures Using a Structurally Dynamic Porous Coordination Polymer**

    SciTech Connect

    Kristi L. Kauffman, Jeffrey T. Culp, Andrew J. Allen, Laura Espinal, Winnie Wong-Ng, Thomas D. Brown, Angela Goodman, Mark P. Bernardo, Russel J. Pancoast, Danielle Chirdon, Christopher Matranga*

    2010-01-01

    The selective adsorption of CO{sub 2} from mixtures with N{sub 2}, CH{sub 4}, and N{sub 2}O in a dynamic porous coordination polymer (see monomer structure) was evaluated by ATR-FTIR spectroscopy, GC, and SANS. All three techniques indicate highly selective adsorption of CO{sub 2} from CO{sub 2}/CH{sub 4} and CO{sub 2}/N{sub 2} mixtures at 30 C, with no selectivity observed for the CO{sub 2}/N{sub 2}O system.

  19. Effect of porous polymer films (track membranes) on the isothermal evaporation kinetics of water

    NASA Astrophysics Data System (ADS)

    Novikov, S. N.; Ermolaeva, A. I.; Timoshenkov, S. P.; Korobova, N. E.; Goryunova, E. P.

    2016-06-01

    The kinetics of isothermal evaporation of distilled water that was in remote (10-15-mm) contact with porous polymer films (track membranes (TMs)) was studied by microgravimetry (derivatograph). When the H2O-TM system contained a disperse medium, the supramolecular structure of water changed, and the number of clusters (coherent domains) drastically decreased. The extraction of the light phase from liquid water was correlated with the chemisorption of H2O molecules containing the para-isomer of hydrogen, which predominantly form coherent domains of water.

  20. Decoding the Morphological Diversity in Two Dimensional Crystalline Porous Polymers by Core Planarity Modulation.

    PubMed

    Halder, Arjun; Kandambeth, Sharath; Biswal, Bishnu P; Kaur, Gagandeep; Roy, Neha Chaki; Addicoat, Matthew; Salunke, Jagadish K; Banerjee, Subhrashis; Vanka, Kumar; Heine, Thomas; Verma, Sandeep; Banerjee, Rahul

    2016-06-27

    Two new chemically stable triazine- and phenyl-core-based crystalline porous polymers (CPPs) have been synthesized using a single-step template-free solvothermal route. Unique morphological diversities were observed for these CPPs [2,3-DhaTta (ribbon) and 2,3-DhaTab (hollow sphere)] by simply altering the linker planarity. A detailed time-dependent study established a significant correlation between the molecular level structures of building blocks with the morphology of CPPs. Moreover, a DFT study was done for calculating the interlayer stacking energy, which revealed that the extent of stacking efficiency is responsible for governing the morphological diversity in these CPPs. PMID:26953562

  1. Separation of gas mixtures using Co(II) carborane-based porous coordination polymers

    SciTech Connect

    Bae, Youn-Sang; Spokoyny, Alexander M.; Farha, Omar K.; Snurr, Randall Q.; Hupp, Joseph T.; Mirkin, Chad A.

    2010-01-01

    Separations of CO{sub 2}/CH{sub 4}, CO{sub 2}/N{sub 2}, and O{sub 2}/N{sub 2} mixtures were studied in three porous coordination polymers made of the same carborane ligand and Co(II) nodes. High selectivities for CO{sub 2} over CH{sub 4} (~47) and CO{sub 2} over N{sub 2} (~95) were obtained, especially in the material with coordinated pyridine. Unusual selectivity for O{sub 2} over N{sub 2} (as high as 6.5) was demonstrated in the materials with open Co(II) sites.

  2. A novel 2D porous indium coordination polymer with tunable luminescent property

    NASA Astrophysics Data System (ADS)

    Li, Xuejiao; Wang, Fangfang; Yang, He; Xu, Bo; Li, Cuncheng

    2016-08-01

    A new Indium coordination polymer [In(pda)1.5(phen)]n1 based on 1,4-phenylenediacetic acid (H2pda) and phen = 1,10-phenanthroline was obtained under hydrothermal condition and further characterized by single crystal X-ray analysis and other physicochemical studies such as infrared spectrum (IR), elemental analysis, thermogravimetric analysis (TGA) and powder X-ray diffraction (PXRD). Structure analysis reveals that complex 1 exhibits 2D porous (6,3) connected layer structure. Luminescent property of 1 was investigated both in the solid state and in different solvents and the results indicated that complex 1 demonstrates distinct solvent dependent luminescent property.

  3. Evaluation of Metal-Organic Frameworks and Porous Polymer Networks for CO2 -Capture Applications.

    PubMed

    Verdegaal, Wolfgang M; Wang, Kecheng; Sculley, Julian P; Wriedt, Mario; Zhou, Hong-Cai

    2016-03-21

    This manuscript presents experimental data for 20 adsorption materials (metal-organic frameworks, porous polymer networks, and Zeolite-5A), including CO2 and N2 isotherms and heat capacities. With input from only experimental data, working capacities per energy for each material were calculated. Furthermore, by running seven different carbon-capture scenarios in which the initial flue-gas composition and process temperature was systematically changed, we present a range of performances for each material and quantify how sensitive each is to these varying parameters. The presented calculations provide researchers with a tool to investigate promising carbon-capture materials more easily and completely. PMID:26840979

  4. An ultra-sensitive microfluidic immunoassay using living radical polymerization and porous polymer monoliths.

    SciTech Connect

    Abhyankar, Vinay V.; Singh, Anup K.; Hatch, Anson V.

    2010-07-01

    We present a platform that combines patterned photopolymerized polymer monoliths with living radical polymerization (LRP) to develop a low cost microfluidic based immunoassay capable of sensitive (low to sub pM) and rapid (<30 minute) detection of protein in 100 {micro}L sample. The introduction of LRP functionality to the porous monolith allows one step grafting of functionalized affinity probes from the monolith surface while the composition of the hydrophilic graft chain reduces non-specific interactions and helps to significantly improve the limit of detection.

  5. Undercutting of defects in thin film protective coatings on polymer surfaces exposed to atomic oxygen

    NASA Technical Reports Server (NTRS)

    Rutledge, Sharon K.; Mihelcic, Judith A.

    1989-01-01

    Protection for polymeric surfaces is needed to make them durable in the low Earth orbital environment, where oxidation by atomic oxygen is the predominant failure mechanism. Thin film coatings of oxides such as silicon dioxide are viable candidates to provide this protection, but concern has been voiced over the ability of these coatings to protect when defects are present in the coating due to surface anomalies occurring during the deposition process, handling, or micrometeoroid and debris bombardment in low Earth orbit. When a defected coating protecting a polymer substrate is exposed to atomic oxygen, the defect provides a pathway to the underlying polymer allowing oxidation and subsequent undercutting to occur. Defect undercutting was studied for sputter deposited coatings of silicon dioxide on polyimide Kapton. Preliminary results indicate that undercutting may be limited as long as the coating remains intact with the substrate. Therefore, coatings may not need to be defect free to give protection to the underlying surface.

  6. Undercutting of defects in thin film protective coatings on polymer surfaces exposed to atomic oxygen

    NASA Technical Reports Server (NTRS)

    Rutledge, Sharon K.; Mihelcic, Judith A.

    1989-01-01

    Protection for polymeric surfaces is needed to make them durable in the low earth orbital environment. Thin film coatings of oxides such as SiO2 are viable candidates to provide this protection, but concern has been voiced over the ability of these coatings to protect when defects are present in the coating due to surface anomalies. When a defected coating protecting a polymer substrate is exposed to atomic oxygen, the defect provides a pathway to the underlying polymer allowing oxidation and subsequent undercutting to occur. Defect undercutting was studied for sputter deposited coatings of SiO2 on polyimide Kapton. Preliminary results indicate that undercutting may be limited as long as the coating remains intact with the substrate. Therefore, coatings may not need to be defect free to give protection to the underlying surface.

  7. Gas turbine ceramic-coated-vane concept with convection-cooled porous metal core

    NASA Technical Reports Server (NTRS)

    Kascak, A. F.; Liebert, C. H.; Handschuh, R. F.; Ludwig, L. P.

    1981-01-01

    Analysis and flow experiments on a ceramic-coated-porous-metal vane concept indicated the feasibility, from a heat transfer standpoint, of operating in a high-temperature (2500 F) gas turbine cascade facility. The heat transfer and pressure drop calculations provided a basis for selecting the ceramic layer thickness (to 0.08 in.), which was found to be the dominant factor in the overall heat transfer coefficient. Also an approximate analysis of the heat transfer in the vane trailing edge revealed that with trailing-edge ejection the ceramic thickness could be reduced to (0.01 in.) in this portion of the vane.

  8. Characterization of pseudo-porous SiC/C coatings on Nextel{trademark}440 and Nicalon{trademark} fibers

    SciTech Connect

    Khasgiwale, N.R.; Butler, E.P.; Tsakalakos, L.; Hensley, D.A.; Cannon, W.R.; Danforth, S.C.; Gonczy, S.T.

    1995-10-01

    Pseudo-porous SiC/C coatings were deposited on Nextel{trademark}440 and Nicalon{trademark} fibers by CVD. The morphology and chemistry of the coatings was evaluated, both before and after oxidation, using Scanning Electron Microscopy (SEM), X-Ray Diffraction Analysis (XRD), X-Ray Photoelectron Spectroscopy (XPS) and Auger spectroscopy. Coated fibers were subjected to two different oxidation treatments to assess coating stability: (a) oxidation at 600 C for 20 hours, and (b) oxidation at 1,000 C for 20 hours. Pseudo-porous SiC/C on Nicalon{trademark} fibers appear to be more oxidation resistant than the same coatings on Nextel{trademark}440 fibers.

  9. A polymer-free Paclitaxel eluting coronary stent: effects of solvents, drug concentrations and coating methods.

    PubMed

    Lamichhane, Sujan; Gallo, Annemarie; Mani, Gopinath

    2014-06-01

    Some polymer coatings used in drug-eluting stents (DES) cause adverse reactions. Hence, the use of self-assembled monolayers (SAMs) as a polymer-free platform to deliver an anti-proliferative drug (paclitaxel-PAT) from 2D metal substrates was previously demonstrated. In this study, we optimized the PAT coating on SAMs coated 3D coronary stents. For the optimization process, we investigated the effects of solvents (ethanol, DMSO, and their mixtures), drug concentrations (2, 3, 4, 8, and 12 mg/mL) in the coating solution, and coating methods (dip and spray) on PAT deposition. A solvent mixture of 75:25 v/v Et-OH:DMSO was determined to be the best for obtaining smooth and homogenous PAT coating. PAT coated stents prepared using 8 mg/mL and 3 mg/mL concentrations of PAT by dip and spray coating methods, respectively, were optimal in terms of carrying adequate drug doses (0.35 µg/mm(2) for dipping and 0.76 µg/mm(2) for spraying) as well as negligible defects observed in the coating. PAT was successfully released from SAMs coated stents in a biphasic manner with an initial burst followed by a sustained release for up to 10 weeks. Thus, this study sheds light on the effects of solvents, drug concentrations, and coating methods on preparing a polymer-free DES. PMID:24705673

  10. Mixed Polymer-Coated Magnetic Nanoparticles as Forward Osmosis Draw Agents of Tuned Hydrophilicity.

    PubMed

    Dey, Priyanka; Izake, Emad L

    2016-08-01

    We recently reported a polymer-coated magnetic nanoparticle (MNP) draw agent for the forward osmosis (FO) water desalination process. The water flux was found to increase when the polymer poly(sodium acrylate) (PSA) was anchored to the MNP surface as compared to the polymer (or polyelectrolyte solution) alone, due to the polymer chains being stretched out and most of the hydrophilic groups on the polymer contributing to water flux. We herein report the use of a secondary polymer poly(N-isopropylacrylamide) PNIPAM to manipulate the PSA polymer conformation and influence inter- and intrachain interactions to enhance the efficiency of the FO draw agent. These PSA-PNIPAM-coated MNPs generated a much higher water flux of ∼11.66 LMH when compared to the 100 % PSA-coated MNPs featuring a value of ∼5.32 LMH under identical FO conditions. The osmotic pressure and water flux driven by the mixed polymer-coated MNPs were found to be a strong function of the net polymer coverage on MNPs, that is, net available hydrophilic groups. Our new draw agent demonstrates potential for use in the water industry due to its improved efficiency and cost effectiveness as it uses only ∼0.062 % (w/v) of the draw agent solution. PMID:27376360

  11. Tantalum coating on porous Ti6Al4V scaffold using chemical vapor deposition and preliminary biological evaluation.

    PubMed

    Li, Xiang; Wang, Lin; Yu, Xiaoming; Feng, Yafei; Wang, Chengtao; Yang, Ke; Su, Daniel

    2013-07-01

    Porous tantalum (Ta), produced via chemical vapor deposition (CVD) of commercially pure Ta onto a vitreous carbon, is currently available for use in orthopedic applications. However, the relatively high manufacturing cost and the incapability to produce customized implant using medical image data have limited its application to gain widespread acceptance. In this study, Ta film was deposited on porous Ti6Al4V scaffolds using CVD technique. Digital microscopy and scanning electron microscopy indicated that the Ta coating evenly covered the entire scaffold structure. X-ray diffraction analysis showed that the coating consisted of α and β phases of Ta. Goat mesenchymal stem cells were seeded and cultured on the Ti6Al4V scaffolds with and without coating. The tetrazolium-based colorimetric assay exhibited better cell adhesion and proliferation on Ta-coated scaffolds compared with uncoated scaffolds. The porous scaffolds were subsequently implanted in goats for 12weeks. Histological analysis revealed similar bone formation around the periphery of the coated and uncoated implants, but bone ingrowth is better within the Ta-coated scaffolds. To demonstrate the ability of producing custom implant for clinical applications via this technology, we designed and fabricated a porous Ti6Al4V scaffold with segmental mandibular shape derived from patient computerized tomography data. PMID:23623123

  12. Optical and topographic changes in water-responsive patterned cholesteric liquid crystalline polymer coatings

    NASA Astrophysics Data System (ADS)

    Stumpel, Jelle E.; Broer, Dirk J.; Bastiaansen, Cees W. M.; Schenning, Albert P. H. J.

    2014-05-01

    In this work, we present patterned water-responsive coatings, which alter both their topological and optical properties. The polymer coatings are based on a hydrogen-bonded cholesteric liquid crystalline polymer network. A two-step photopolymerization procedure leads to a patterned coating with repeating liquid crystalline and isotropic areas. The cholesteric liquid crystalline areas reflect green light, whilst the isotropic areas are transparent for visible light. Treatment with alkaline solution results in a hygroscopic polymer salt coating. When placed in demineralized water, the polymer films swells, leading to an enhancement of the surface topography structure in which the liquid crystalline areas swell more. Moreover, the pitch of the helical organization in the cholesteric areas increases due to this swelling leading to a color change from green to red.

  13. Nanoparticle-Functionalized Porous Polymer Monolith Detection Elements for Surface-Enhanced Raman Scattering

    PubMed Central

    Liu, Jikun; White, Ian; DeVoe, Don L.

    2011-01-01

    The use of porous polymer monoliths functionalized with silver nanoparticles is introduced in this work for high-sensitivity surface-enhanced Raman scattering (SERS) detection. Preparation of the SERS detection elements is a simple process comprising the synthesis of a discrete polymer monolith section within a silica capillary, followed by physically trapping silver nanoparticle aggregates within the monolith matrix. A SERS detection limit of 220 fmol for Rhodamine 6G (R6G) is demonstrated, with excellent signal stability over a 24 h period. The capability of the SERS-active monolith for label-free detection of biomolecules was demonstrated by measurements of bradykinin and cyctochrome c. The SERS-active monoliths can be readily integrated into miniaturized micro-total-analysis systems for on-line and label-free detection for a variety of biosensing, bioanalytical, and biomedical applications. PMID:21322579

  14. The contribution of the nonporous distal stem to the stability of proximally porous-coated canine femoral components.

    PubMed

    Jasty, M; Krushell, R; Zalenski, E; O'Connor, D; Sedlacek, R; Harris, W

    1993-02-01

    The contribution of the distal nonporous-coated stem to the stability of the uncemented femoral components, which were porous coated only proximally, was investigated under two conditions: (1) immediately after insertion and (2) at 6 months, 1 year, and 2 years after surgery in a canine model. The relative motion of the femoral components at the bone porous-coating interface under loads simulating the canine midstance was measured at these time periods using displacement transducers. The measurements were repeated after severing the connection between the porous-coated proximal body and the nonporous-coated distal stem through a small hole in the anterior cortex. The results showed that while the distal nonporous-coated stem enhanced the immediate stability of the proximally porous-coated uncemented femoral components, it contributed little to the long-term stability of the femoral components after bony ingrowth had occurred in vivo. The mean relative motion between the body of the prosthesis and the cortical bone increased from 12 microns (+/- 7 microns) to 31 microns (+/- 34 microns) in the posterior transverse direction when the stem was immediately severed after the surgery. However, at 6 months, 1 year, and 2 years after surgery, extensive bone ingrowth had occurred into the proximal porous-coated regions of the body and provided excellent stability to the femoral components. With bone ingrowth, the mean relative motion was less than 5 microns at any site. Under these conditions, severing the stem did not increase the relative motion of the prostheses significantly.(ABSTRACT TRUNCATED AT 250 WORDS) PMID:8436987

  15. Enhanced electrochemical performance of Lithium-ion batteries by conformal coating of polymer electrolyte

    PubMed Central

    2014-01-01

    This work reports the conformal coating of poly(poly(ethylene glycol) methyl ether methacrylate) (P(MePEGMA)) polymer electrolyte on highly organized titania nanotubes (TiO2nts) fabricated by electrochemical anodization of Ti foil. The conformal coating was achieved by electropolymerization using cyclic voltammetry technique. The characterization of the polymer electrolyte by proton nuclear magnetic resonance (1H NMR) and size-exclusion chromatography (SEC) shows the formation of short polymer chains, mainly trimers. X-ray photoelectron spectroscopy (XPS) results confirm the presence of the polymer and LiTFSI salt. The galvanostatic tests at 1C show that the performance of the half cell against metallic Li foil is improved by 33% when TiO2nts are conformally coated with the polymer electrolyte. PMID:25317101

  16. Manufacture of porous biodegradable polymer conduits by an extrusion process for guided tissue regeneration

    NASA Technical Reports Server (NTRS)

    Widmer, M. S.; Gupta, P. K.; Lu, L.; Meszlenyi, R. K.; Evans, G. R.; Brandt, K.; Savel, T.; Gurlek, A.; Patrick, C. W. Jr; Mikos, A. G.; McIntire, L. V. (Principal Investigator)

    1998-01-01

    We have fabricated porous, biodegradable tubular conduits for guided tissue regeneration using a combined solvent casting and extrusion technique. The biodegradable polymers used in this study were poly(DL-lactic-co-glycolic acid) (PLGA) and poly(L-lactic acid) (PLLA). A polymer/salt composite was first prepared by a solvent casting process. After drying, the composite was extruded to form a tubular construct. The salt particles in the construct were then leached out leaving a conduit with an open-pore structure. PLGA was studied as a model polymer to analyze the effects of salt weight fraction, salt particle size, and processing temperature on porosity and pore size of the extruded conduits. The porosity and pore size were found to increase with increasing salt weight fraction. Increasing the salt particle size increased the pore diameter but did not affect the porosity. High extrusion temperatures decreased the pore diameter without altering the porosity. Greater decrease in molecular weight was observed for conduits manufactured at higher temperatures. The mechanical properties of both PLGA and PLLA conduits were tested after degradation in vitro for up to 8 weeks. The modulus and failure strength of PLLA conduits were approximately 10 times higher than those of PLGA conduits. Failure strain was similar for both conduits. After degradation for 8 weeks, the molecular weights of the PLGA and PLLA conduits decreased to 38% and 43% of the initial values, respectively. However, both conduits maintained their shape and did not collapse. The PLGA also remained amorphous throughout the time course, while the crystallinity of PLLA increased from 5.2% to 11.5%. The potential of seeding the conduits with cells for transplantation or with biodegradable polymer microparticles for drug delivery was also tested with dyed microspheres. These porous tubular structures hold great promise for the regeneration of tissues which require tubular scaffolds such as peripheral nerve

  17. Polymer coating for immobilizing soluble ions in a phosphate ceramic product

    DOEpatents

    Singh, Dileep; Wagh, Arun S.; Patel, Kartikey D.

    2000-01-01

    A polymer coating is applied to the surface of a phosphate ceramic composite to effectively immobilize soluble salt anions encapsulated within the phosphate ceramic composite. The polymer coating is made from ceramic materials, including at least one inorganic metal compound, that wet and adhere to the surface structure of the phosphate ceramic composite, thereby isolating the soluble salt anions from the environment and ensuring long-term integrity of the phosphate ceramic composite.

  18. Polymer Coating for Immobilizing Soluble Ions in a Phosphate Ceramic Product

    SciTech Connect

    Singh, Dileep; Wagh, Arun S.; Patel, Kartikey D.

    1999-05-05

    A polymer coating is applied to the surface of a phosphate ceramic composite to effectively immobilize soluble salt anions encapsulated within the phosphate ceramic composite. The polymer coating is made from ceramic materials, including at least one inorganic metal compound, that wet and adhere to the surface structure of the phosphate ceramic composite, thereby isolating the soluble salt anions from the environment and ensuring long-term integrity of the phosphate ceramic composite.

  19. Organometallic Polymer Coatings for Geothermal-Fluid-Sprayed Air-Cooled Condensers: Preprint

    SciTech Connect

    Gawlik, K.; Sugama, T.; Jung, D.

    2002-08-01

    Researchers are developing polymer-based coating systems to reduce scaling and corrosion of air-cooled condensers that use a geothermal fluid spray for heat transfer augmentation. These coating systems act as barriers to corrosion to protect aluminum fins and steel tubing; they are formulated to resist the strong attachment of scale. Field tests have been done to determine the corrosion and scaling issues related to brine spraying and a promising organometallic polymer has been evaluated in salt spray tests.

  20. Investigations of conductive polymer coatings for corrosion protection of aluminum alloys

    NASA Astrophysics Data System (ADS)

    Racicot, Robert James

    The anti-corrosion properties of a novel double strand conductive polymer coating on aluminum alloys in salt environments as a possible replacement for chromium conversion coatings was investigated. The conductive coating consisted of a double helix backbone structure of polyaniline wrapped with an esterified polyacrylic acid strand. This polymer complex offers advantages over other conductive polymer systems in material stability and processability. The polymer is soluble in single organic solvents and was sprayed onto square AA7075-T6 and AA2024-T3 aluminum alloy samples. The coatings were investigated for corrosion protection properties using cyclic polarization, electrochemical impedance spectroscopy (EIS) and long term exposure in aggressive salt environments. The polymer coated samples were tested against two commercial chromate conversion coatings and uncoated alloy samples. The cyclic polarization tests show a two order of magnitude lowering of the corrosion current over the uncoated samples, a one order of magnitude lowering of Isbcorr over the second type of chromate coating and a one order of magnitude higher Isbcorr over the first type of chromate coating. Impedance results show a two order of magnitude higher impedance at low frequencies over the uncoated and equivalent performance for both types of chromate coatings. EIS and cyclic polarization tests of the conductive state (green colored) versus a non-conductive state (blue colored) of the polymer coating shows that the electrically conductive state is more effective than the insulating state for corrosion protection. This data indicates that the electro-active nature of the polymer coating plays a role in the protection of the alloys. After two months exposure in a.5N NaCl solution, there is no evidence of pitting at the alloy surface for the polymer coated samples under scanning electron microscopy (SEM) images, indicating a change in the typical corrosion mechanism for aluminum alloys. The

  1. Enhanced Surface Interaction of Water Confined in Hierarchical Porous Polymers Induced by Hydrogen Bonding.

    PubMed

    Silletta, Emilia V; Velasco, Manuel I; Gomez, Cesar G; Strumia, Miriam C; Stapf, Siegfried; Mattea, Carlos; Monti, Gustavo A; Acosta, Rodolfo H

    2016-07-26

    Hierarchical porous polymer systems are increasingly applied to catalysis, bioengineering, or separation technology because of the versatility provided by the connection of mesopores with percolating macroporous structures. Nuclear magnetic resonance (NMR) is a suitable technique for the study of such systems as it can detect signals stemming from the confined liquid and translate this information into pore size, molecular mobility, and liquid-surface interactions. We focus on the properties of water confined in macroporous polymers of ethylene glycol dimethacrylate and 2-hydroxyethyl methacrylate [poly(EGDMA-co-HEMA)] with different amounts of cross-linkers, in which a substantial variation of hydroxyl groups is achieved. As soft polymer scaffolds may swell upon saturation with determined liquids, the use of NMR is particularly important as it measures the system in its operational state. This study combines different NMR techniques to obtain information on surface interactions of water with hydrophilic polymer chains. A transition from a surface-induced relaxation in which relaxivity depends on the pore size to a regime where the organic pore surface strongly restricts water diffusion is observed. Surface affinities are defined through the molecular residence times near the network surface. PMID:27341270

  2. Toward compositional design of reticular type porous films by mixing and coating titania-based frameworks with silica

    NASA Astrophysics Data System (ADS)

    Kimura, T.

    2015-12-01

    A recently developed reticular type porous structure, which can be fabricated as the film through the soft colloidal block copolymer (e.g., PS-b-PEO) templating, is very promising as the porous platform showing high-performance based on its high surface area as well as high diffusivity of targeted organic molecules and effective accommodation of bulky molecules, but the compositional design of oxide frameworks has not been developed so enough to date. Here, I report reliable synthetic methods of the reticular type porous structure toward simple compositional variations. Due to the reproducibility of reticular type porous titania films from titanium alkoxide (e.g., TTIP; titanium tetraisopropoxide), a titania-silica film having similar porous structure was obtained by mixing silicon alkoxide (e.g., tetraethoxysilane) and TTIP followed by their pre-hydrolysis, and the mixing ratio of Ti to Si composition was easily reached to 1.0. For further compositional design, a concept of surface coating was widely applicable; the reticular type porous titania surfaces can be coated with other oxides such as silica. Here, a silica coating was successfully achieved by the simple chemical vapor deposition of silicon alkoxide (e.g., tetramethoxysilane) without water (with water at the humidity level), which was also utilized for pore filling with silica by the similar process with water.

  3. A mesomechanical analysis of the deformation and fracture in polycrystalline materials with ceramic porous coatings

    NASA Astrophysics Data System (ADS)

    Balokhonov, R. R.; Zinoviev, A. V.; Romanova, V. A.; Batukhtina, E. E.

    2015-10-01

    The special features inherent in the mesoscale mechanical behavior of a porous ceramic coating-steel substrate composite are investigated. Microstructure of the coated material is accounted for explicitly as initial conditions of a plane strain dynamic boundary-value problem solved by the finite difference method. Using a mechanical analogy method, a procedure for generating a uniform curvilinear finite difference computational mesh is developed to provide a more accurate description of the complex grain boundary geometry. A modified algorithm for generation of polycrystalline microstructure of the substrate is designed on the basis of the cellular automata method. The constitutive equations for a steel matrix incorporate an elastic-plastic model for a material subjected to isotropic hardening. The Hall-Petch relation is used to account for the effect of the grain size on the yield stress and strain hardening history. A brittle fracture model for a ceramic coating relying on the Huber criterion is employed. The model allows for crack nucleation in the regions of triaxial tension. The complex inhomogeneous stress and plastic strain patterns are shown to be due to the presence of interfaces of three types: coating-substrate interface, grain boundaries, and pore surfaces.

  4. Preparation and characterization of porous carbon material-coated solid-phase microextraction metal fibers.

    PubMed

    Zhu, Fang; Guo, Jiaming; Zeng, Feng; Fu, Ruowen; Wu, Dingcai; Luan, Tiangang; Tong, Yexiang; Lu, Tongbu; Ouyang, Gangfeng

    2010-12-10

    Two kinds of porous carbon materials, including carbon aerogels (CAs), wormhole-like mesoporous carbons (WMCs), were synthesized and used as the coatings of solid-phase microextraction (SPME) fibers. By using stainless steel wire as the supporting core, six types of fibers were prepared with sol-gel method, direct coating method and direct coating plus sol-gel method. Headspace SPME experiments indicated that the extraction efficiencies of the CA fibers are better than those of the WMC fibers, although the surface area of WMCs is much higher than that of CAs. The sol-gel-CA fiber (CA-A) exhibited excellent extraction properties for non-polar compounds (BTEX, benzene, toluene, ethylbenzene, o-xylene), while direct-coated CA fiber (CA-B) presented the best performance in extracting polar compounds (phenols). The two CA fibers showed wide linear ranges, low detection limits (0.008-0.047μgL(-1) for BTEX, 0.15-5.7μgL(-1) for phenols) and good repeatabilities (RSDs less than 4.6% for BTEX, and less than 9.5% for phenols) and satisfying reproducibilities between fibers (RSDs less than 5.2% for BTEX, and less than 9.9% for phenols). These fibers were successfully used for the analysis of water samples from the Pearl River, which demonstrated the applicability of the home-made CA fibers. PMID:21074162

  5. Adhesion Issues with Polymer/Oxide Barrier Coatings on Organic Displays

    SciTech Connect

    Matson, Dean W.; Martin, Peter M.; Graff, Gordon L.; Gross, Mark E.; Burrows, Paul E.; Bennett, Wendy D.; Hall, Michael G.; Mast, Eric S.; Bonham, Charles C.; Zumhoff, Mac R.; Rutherford, Nicole M.; Moro, Lorenza; Rosenblum, Martin; Praino, Robert F.; Visser, Robert J.

    2005-01-01

    Multilayer polymer/oxide coatings are being developed to protect sensitive organic display devices, such as OLEDs, from oxygen and water vapor permeation. The coatings have permeation levels ~ 10-6 g/m2/d for water vapor and ~10-6 cc/m2/d for oxygen, and are deposited by vacuum polymer technology. The coatings consist of either a base Al2O3 or acrylate polymer adhesion layer followed by alternating Al2O3/polymer layers. The polymer is used to decouple the 30 nm-thick Al2O3 barrier layers. Adhesion of the barrier coating to the substrate and display device is critical for the operating lifetime of the device. The substrate material could be any transparent flexible plastic. The coating technology can also be used to encapsulate organic-based electronic devices to protect them from atmospheric degradation. Plasma pretreatment is also needed for good adhesion to the substrate, but if it is too aggressive, it will damage the organic display device. We report on the effects of plasma treatment on the adhesion of barrier coatings to plastic substrates and the performance of OLED devices after plasma treatment and barrier coating deposition. We find that initial OLED performance is not significantly affected by the deposition process and plasma treatment, as demonstrated by luminosity and I-V curves.

  6. Analysis of gas transport in polymer electrolyte fuel cells using porous structure constructed from X-ray nano CT

    NASA Astrophysics Data System (ADS)

    Kinefuchi, Ikuya; Oyama, Junpei; Yokoyama, Koji; Kubo, Norio; Tokumasu, Takashi; Matsumoto, Yoichiro

    2013-03-01

    This paper describes the analysis of gas transport in micro porous layers of polymer electrolyte fuel cells based on the three-dimensional structure obtained from X-ray nano computed tomography (CT). The polygonal surface representation of the porous structure was constructed from the cross-sectional CT images using the marching tetrahedrons algorithm. The diffusion flux through the porous layer was evaluated by the direct simulation Monte Carlo method since the characteristic pore size is comparable to the mean free path of gas molecules. The numerical simulation well reproduces the experimentally observed pressure dependence of diffusion resistance originating from the transition between Knudsen and molecular diffusion regimes. The effect of porous media morphology on gas transport was examined by an analysis of the trajectories of transmitted molecules through the porous layer. This work was partially supported by New Energy and Industrial Technology Development Organization (NEDO) of Japan.

  7. Piezoelectric biosensor with a ladder polymer substrate coating

    DOEpatents

    Renschler, Clifford L.; White, Christine A.; Carter, Robert M.

    1998-01-01

    A piezoelectric biosensor substrate useful for immobilizing biomolecules in an oriented manner on the surface of a piezoelectric sensor has a ladder polymer of polyacrylonitrile. To make the substrate, a solution of an organic polymer, preferably polyacrylonitrile, is applied to the surface of a piezoelectric sensor. The organic polymer is modifying by heating the polymer in a controlled fashion in air such that a ladder polymer is produced which, in turn, forms the attachment point for the biomolecules comprising the piezoelectric biosensor.

  8. Porous Silica-Coated Gold Nanorods: A Highly Active Catalyst for the Reduction of 4-Nitrophenol.

    PubMed

    Mohanta, Jagdeep; Satapathy, Smithsagar; Si, Satyabrata

    2016-02-01

    The successful coating of thin porous silica layers of various thicknesses [(10±1), (12±1), and (14±1) nm] on cetyl trimethylammonium bromide (CTAB) capped gold nanorods was achieved through a modified Stöber procedure. The resulting material was applied as a novel catalyst for the reduction of 4-nitrophenol. The catalytic activities of the gold nanorods increased up to eight times after coating with a layer of porous silica and the reaction followed a zero-order kinetics, having a rate constant as high as 2.92×10(-1) mol L(-1) min(-1). The spectral changes during the reduction reaction of 4-nitrophenol were observed within a very short span of time and a complete conversion to 4-aminophenol occured within 5-6 mins, including the induction period of ≈2 mins. The reusability of the catalyst was studied by running the catalytic reaction during five consecutive cycles with good efficiency without destroying the nanostructure. The methodology can be effectively applied to the development of composite catalysts with highly enhanced catalytic activity. PMID:26663755

  9. Etiology of osteolysis around porous-coated cementless total hip arthroplasties.

    PubMed

    Jasty, M; Bragdon, C; Jiranek, W; Chandler, H; Maloney, W; Harris, W H

    1994-11-01

    The prosthetic components and tissues retrieved from 12 hips with osteolysis in association with well-fixed cementless porous-coated total hip prostheses (5 Porous Coated Anatomic, 6 Harris-Galante Porous, and 1 Omniflex) were examined using a variety specific techniques including electron microscopy, standard histology, immunohistochemistry, and particle identification. The patients were young and active. Extensive osteolysis developed in all 12 femurs and 3 acetabula between 36 and 84 months after arthroplasty (mean, 63 months). All of the polyethylene liners were noted to be worn substantially (mean volumetric wear, 1140 +/- 810 mm3). The wear was unrelated to the head diameter in this small number of cases. In all 12 cases, the articulating surfaces were wear polished and contained numerous fine multidirectional scratches, suggesting 3-body abrasive wear mechanisms in addition to adhesive wear liberating very small (micron to submicron) wear particles. In 4 cases, surface delamination and flaking of polyethylene were also found, suggesting fatigue wear liberating larger wear particles. Nine of 10 cobalt alloy heads showed numerous fine scratches with sharp edges presumably from 3-body abrasive wear. Corrosion and fretting at the femoral head-neck junction in 5 cases, burnishing of the femoral stem against bone in 4 cases, and metal staining of tissues opposite the porous coatings in 7 cases provided evidence for the liberation of fine metal particles from outside the articulation. Histologic and immunohistochemical studies of tissue in the regions of osteolysis in all cases showed numerous focal aggregates of KP1 antibody positive activated macrophages containing large amounts of submicron intracellular particles of polyethylene (presumably related to the 3-body abrasive wear polishing) and giant cells within a fibrous stroma. In 5 cases, some of the macrophages also contained submicron metal particles but smaller in numbers. T lymphocytes, plasma cells, and

  10. Trypsin immobilization in ordered porous polymer membranes for effective protein digestion.

    PubMed

    Qiao, Juan; Kim, Jin Yong; Wang, Yuan Yuan; Qi, Li; Wang, Fu Yi; Moon, Myeong Hee

    2016-02-01

    Fast and effective protein digestion is a vital process for mass spectrometry (MS) based protein analysis. This study introduces a porous polymer membrane enzyme reactor (PPMER) coupled to nanoflow liquid chromatography-tandem MS (nLC-ESI-MS/MS) for on-line digestion and analysis of proteins. Poly (styrene-co-maleic anhydride) (PS-co-MAn) was fabricated by the breath figure method to make a porous polymer membrane in which the MAn group was covalently bound to enzyme. Based on this strategy, microscale PPMER (μPPMER) was constructed for on-line connection with the nLC-ESI-MS/MS system. Its capability for enzymatic digestion with bovine serum albumin (BSA) was evaluated with varied digestion periods. The on-line proteolysis of BSA and subsequent analysis with μPPMER-nLC-ESI-MS/MS revealed that peptide sequence coverage increased from 10.3% (digestion time 10 min) to 89.1% (digestion time 30 min). μPPMER can efficiently digest proteins due to the microscopic confinement effect, showing its potential application in fast protein identification and protease immobilization. Applications of on-line digestion using μPPMER with human plasma and urinary proteome samples showed that the developed on-line method yielded equivalent or better performance in protein coverage and identified more membrane proteins than the in-solution method. This may be due to easy accommodation of hydrophobic membrane proteins within membrane pores. PMID:26772135

  11. Porous antioxidant polymer microparticles as therapeutic systems for the airway inflammatory diseases.

    PubMed

    Jeong, Dahee; Kang, Changsun; Jung, Eunkyeong; Yoo, Donghyuck; Wu, Dongmei; Lee, Dongwon

    2016-07-10

    Inhaling steroidal anti-inflammatory drugs is the most common treatment for airway inflammatory diseases such as asthma. However, frequent steroid administration causes adverse side effects. Therefore, the successful clinical translation of numerous steroidal drugs greatly needs pulmonary drug delivery systems which are formulated from biocompatible and non-immunogenic polymers. We have recently developed a new family of biodegradable polymer, vanillyl alcohol-containing copolyoxalate (PVAX) which is able to scavenge hydrogen peroxide and exert potent antioxidant and anti-inflammatory activity. In this work, we report the therapeutic potential of porous PVAX microparticles which encapsulate dexamethasone (DEX) as a therapeutic system for airway inflammatory diseases. PVAX microparticles themselves reduced oxidative stress and suppressed the expression of pro-inflammatory tumor necrosis factor-alpha and inducible nitric oxide synthase in the lung of ovalbumin-challenged asthmatic mice. However, DEX-loaded porous PVAX microparticles showed significantly enhanced therapeutic effects than PVAX microparticles, suggesting the synergistic effects of PVAX with DEX. In addition, PVAX microparticles showed no inflammatory responses to lung tissues. Given their excellent biocompatibility and intrinsic antioxidant and anti-inflammatory activity, PVAX microparticles hold tremendous potential as therapeutic systems for the treatment of airway inflammatory diseases such as asthma. PMID:27151077

  12. Highly porous organic polymers bearing tertiary amine group and their exceptionally high CO2 uptake capacities

    NASA Astrophysics Data System (ADS)

    Gomes, Ruth; Bhaumik, Asim

    2015-02-01

    We report a very simple and unique strategy for synthesis of a tertiary amine functionalized high surface area porous organic polymer (POP) PDVTA-1 through the co-polymerization of monomers divinylbenzene (DVB) and triallylamine (TAA) under solvothermal reaction conditions. Two different PDVTA-1 samples have been synthesized by varying the molar ratio of the monomers. The porous polymeric materials have been thoroughly characterized by solid state 13C CP MAS-NMR, FT-IR and UV-vis spectroscopy, N2 sorption, HR TEM and FE SEM to understand its chemical environment, nanostructure, bonding, morphology and related surface properties. PDVTA-1 with higher amine content (DVB/TAA=4.0) showed exceptionally high CO2 uptake capacity of 85.8 wt% (19.5 mmol g-1) at 273 K and 43.69 wt% (9.93 mmol g-1) at 298 K under 3 bar pressure, whereas relatively low amine loaded material (DVB/TAA=7.0) shows uptake capacity of 59.2 wt% (13.45 mmol g-1) at 273 K and 34.36 wt% (7.81 mmol g-1) at 298 K. Highly porous nanostructure together with very high surface area and basicity at the surface due to the presence of abundant basic tertiary amine N-sites in the framework of PDVTA-1 could be responsible for very high CO2 adsorption.

  13. Porous coordination polymers as novel sorption materials for heat transformation processes.

    PubMed

    Janiak, Christoph; Henninger, Stefan K

    2013-01-01

    Porous coordination polymers (PCPs)/metal-organic frameworks (MOFs) are inorganic-organic hybrid materials with a permanent three-dimensional porous metal-ligand network. PCPs or MOFs are inorganic-organic analogs of zeolites in terms of porosity and reversible guest exchange properties. Microporous water-stable PCPs with high water uptake capacity are gaining attention for low temperature heat transformation applications in thermally driven adsorption chillers (TDCs) or adsorption heat pumps (AHPs). TDCs or AHPs are an alternative to traditional air conditioners or heat pumps operating on electricity or fossil fuels. By using solar or waste heat as the operating energy TDCs or AHPs can significantly help to minimize primary energy consumption and greenhouse gas emissions generated by industrial or domestic heating and cooling processes. TDCs and AHPs are based on the evaporation and consecutive adsorption of coolant liquids, preferably water, under specific conditions. The process is driven and controlled by the microporosity and hydrophilicity of the employed sorption material. Here we summarize the current investigations, developments and possibilities of PCPs/MOFs for use in low-temperature heat transformation applications as alternative materials for the traditional inorganic porous substances like silica gel, aluminophosphates or zeolites. PMID:23945102

  14. Critical conditions of polymer adsorption and chromatography on non-porous substrates.

    PubMed

    Cimino, Richard T; Rasmussen, Christopher J; Brun, Yefim; Neimark, Alexander V

    2016-07-15

    We present a novel thermodynamic theory and Monte Carlo simulation model for adsorption of macromolecules to solid surfaces that is applied for calculating the chain partition during separation on chromatographic columns packed with non-porous particles. We show that similarly to polymer separation on porous substrates, it is possible to attain three chromatographic modes: size exclusion chromatography at very weak or no adsorption, liquid adsorption chromatography when adsorption effects prevail, and liquid chromatography at critical conditions that occurs at the critical point of adsorption. The main attention is paid to the analysis of the critical conditions, at which the retention is chain length independent. The theoretical results are verified with specially designed experiments on isocratic separation of linear polystyrenes on a column packed with non-porous particles at various solvent compositions. Without invoking any adjustable parameters related to the column and particle geometry, we describe quantitatively the observed transition between the size exclusion and adsorption separation regimes upon the variation of solvent composition, with the intermediate mode occurring at a well-defined critical point of adsorption. A relationship is established between the experimental solvent composition and the effective adsorption potential used in model simulations. PMID:27089017

  15. New Approach to Ceramic/Metal-Polymer Multilayered Coatings for High Performance Dry Sliding Applications

    NASA Astrophysics Data System (ADS)

    Rempp, A.; Killinger, A.; Gadow, R.

    2012-06-01

    The combination of thermally sprayed hard coatings with a polymer based top coat leads to multilayered coating systems with tailored functionalities concerning wear resistance, friction, adhesion, wettability or specific electrical properties. The basic concept is to combine the mechanical properties of the hard base coating with the tribological or chemical abilities of the polymer top coat suitable for the respective application. This paper gives an overview of different types of recently developed multilayer coatings and their application in power transmission under dry sliding conditions. State of the art coatings for dry sliding applications in power transmission are mostly based on thin film coatings like diamond-like carbon or solid lubricants, e.g. MoS2. A new approach is the combination of thin film coatings with combined multilayer coatings. To evaluate the capability of these tribological systems, a multi-stage investigation has been carried out. In the first stage the performance of the sliding lacquers and surface topography of the steel substrate has been evaluated. In the following stage thermally sprayed hard coatings were tested in combination with different sliding lacquers. Wear resistance and friction coefficients of combined coatings were determined using a twin disc test-bed.

  16. Thermal and flow analysis of a convection air-cooled ceramic coated porous metal concept for turbine vanes

    NASA Technical Reports Server (NTRS)

    Stepka, F. S.

    1981-01-01

    The heat transfer and pressure drop through turbine vanes made of a sintered, porous metal coated with a thin layer of ceramic and convection cooled by spanwise flow of cooling air were analyzed. The analysis was made to determine the feasibility of using this concept for cooling very small turbines, primarily for short duration applications such as in missile engines. The analysis was made for gas conditions of approximately 10 and 40 atm and 1644 K and with turbine vanes made of felt type porous metals with relative densities from 0.2 to 0.6 and ceramic coating thicknesses of 0.076 to 0.254 mm.

  17. Fabrication and operation of a system for the PVA (polyvinyl alcohol) coating of polymer microshells with trace gas fill

    SciTech Connect

    King, K.J.

    1988-03-31

    Polymer microshells with a PVA (polyvinyl alcohol) coating are produced for the ICF Program by the Fusion Target Fabrication (FTF) Group at Lawrence Livermore National Laboratories. A PVA coating greatly reduces the permeation of gas through a polymer microshell. The equipment and procedures used in the production of PVA coated microshells are discussed. 6 figs.

  18. Theoretical considerations of the influence of polymer film coatings on the mechanical strength of tablets.

    PubMed

    Stanley, P; Rowe, R C; Newton, J M

    1981-09-01

    A theoretical analysis of the influence of polymer film coatings on the mechanical strength of tablets has been undertaken. Making some basic assumptions, the theory predicts that neither the thickness of the substrate nor that of the coating has any influence on which fractures first, this being solely determined by the ratio of the tensile fracture strength to the Young's modulus for the two materials. Such a finding suggests that in practice for film-coated tablets the substrate will usually fracture before the coating. Simple measurements of maximum failure loads are of little value in assessing the influence of film coating on the mechanical strength of tablets. PMID:6117631

  19. Radioisotope albedo thickness gauging of polymer coatings on a metallic substrate

    SciTech Connect

    Kapranov, B.I.; Myakin 'Kova, L.V.; Shaverin, V.A.

    1986-12-01

    This paper presents results of theoretical and experimental analysis of the possibilities of albedo thickness gauging of the polymer coating on metals. The ranges of measured coating thickness and their relationship with the thickness of the substrate for aluminum, copper, steel, and lead using Pm 147, Am 241, Cd 109, and Co 57 radionuclides as readiation sources are presented.

  20. Preparation of polymer-coated separators using an electron beam irradiation

    NASA Astrophysics Data System (ADS)

    Sohn, Joon-Yong; Gwon, Sung-Jin; Choi, Jae-Hak; Shin, Junhwa; Nho, Young-Chang

    2008-12-01

    A polymer-coated polyethylene (PE) separator was prepared by a dip-coating of PVDF-HFP/PEGDMA on both sides of a PE separator followed by an electron beam irradiation. The thermal and electrochemical properties of the polymer-coated PE separator were investigated by using FT-IR, SEM, DSC and an impedance analyzer. The results showed that the coated PVDF-HFP/PEGDMA layer was covalently bound to the PE separator and also crosslinked by an electron beam irradiation. Thermal shrinkage dramatically decreased with an increase in the absorption dose and the PEGDMA content due to the crosslinking of the coated PVDF-HFP/PEGDMA by an irradiation. The PE separator coated with the composition of PVDF-HFP/PEGDMA (9.5/0.5) and irradiated to 150 kGy showed the highest electrolyte uptake of 125% and ionic conductivity of 3.82 × 10 -4 S/cm at room temperature.

  1. Polydopamine-Coated Porous Substrates as a Platform for Mineralized β-FeOOH Nanorods with Photocatalysis under Sunlight.

    PubMed

    Zhang, Chao; Yang, Hao-Cheng; Wan, Ling-Shu; Liang, Hong-Qing; Li, Hanying; Xu, Zhi-Kang

    2015-06-01

    Immobilization of photo-Fenton catalysts on porous materials is crucial to the efficiency and stability for water purification. Here we report polydopamine (PDA)-coated porous substrates as a platform for in situ mineralizing β-FeOOH nanorods with enhanced photocatalytic performance under sunlight. The PDA coating plays multiple roles as an adhesive interface, a medium inducing mineral generation, and an electron transfer layer. The mineralized β-FeOOH nanorods perfectly wrap various porous substrates and are stable on the substrates that have a PDA coating. The immobilized β-FeOOH nanorods have been shown to be efficient for degrading dyes in water via a photo-Fenton reaction. The degradation efficiency reaches approximately 100% in 60 min when the reaction was carried out with H2O2 under visible light, and it remains higher than 90% after five cycles. We demonstrate that the PDA coating promotes electron transfer to reduce the electron-hole recombination rate. As a result, the β-FeOOH nanorods wrapped on the PDA-coated substrates show enhanced photocatalytic performance under direct sunlight in the presence of H2O2. Moreover, this versatile platform using porous materials as the substrate is useful in fabricating β-FeOOH nanorods-based membrane reactor for wastewater treatment. PMID:25969860

  2. Bone Tissue Response to Porous and Functionalized Titanium and Silica Based Coatings

    PubMed Central

    Chaudhari, Amol; Braem, Annabel; Vleugels, Jozef; Martens, Johan A.; Naert, Ignace; Cardoso, Marcio Vivan; Duyck, Joke

    2011-01-01

    Background Topography and presence of bio-mimetic coatings are known to improve osseointegration. The objective of this study was to evaluate the bone regeneration potential of porous and osteogenic coatings. Methodology Six-implants [Control (CTR); porous titanium coatings (T1, T2); thickened titanium (Ti) dioxide layer (TiO2); Amorphous Microporous Silica (AMS) and Bio-active Glass (BAG)] were implanted randomly in tibiae of 20-New Zealand white rabbits. The animals were sacrificed after 2 or 4 weeks. The samples were analyzed histologically and histomorphometrically. In the initial bone-free areas (bone regeneration areas (BRAs)), the bone area fraction (BAF) was evaluated in the whole cavity (500 µm, BAF-500), in the implant vicinity (100 µm, BAF-100) and further away (100–500 µm, BAF-400) from the implant. Bone-to-implant contact (BIC-BAA) was measured in the areas where the implants were installed in contact to the host bone (bone adaptation areas (BAAs)) to understand and compare the bone adaptation. Mixed models were used for statistical analysis. Principal Findings After 2 weeks, the differences in BAF-500 for different surfaces were not significant (p>0.05). After 4 weeks, a higher BAF-500 was observed for BAG than CTR. BAF-100 for AMS was higher than BAG and BAF-400 for BAG was higher than CTR and AMS. For T1 and AMS, the bone regeneration was faster in the 100-µm compared to the 400-µm zone. BIC-BAA for AMS and BAG was lower after 4 than 2 weeks. After 4 weeks, BIC-BAA for BAG was lower than AMS and CTR. Conclusions BAG is highly osteogenic at a distance from the implant. The porous titanium coatings didn't stimulate bone regeneration but allowed bone growth into the pores. Although AMS didn't stimulate higher bone response, it has a potential of faster bone growth in the vicinity compared to further away from the surface. BIC-BAA data were inconclusive to understand the bone adaptation. PMID:21935382

  3. Molding P3HT conjugated polymer in fibers by solvent-annealing-induced nanowetting in porous template

    NASA Astrophysics Data System (ADS)

    Cidade, Fernando N.; de Deus, Jeferson F.; Macedo, Andreia G.

    2015-07-01

    In this work, poly[3-hexyl-thiophene] (P3HT) polymer was assembled in fibers-like structures using a post-deposition treatment denoted as solvent-annealing-induced nanowetting in templates (SAINT). In this procedure, the as cast P3HT films deposited onto glass (or flexible) substrate are placed in contact with a porous template for instance, anodic alumina oxide (AAO), and then exposed to an atmosphere saturated with vapors of an organic solvent. This will induce a partial dissolution of the polymer and infiltration into the porous. After this, the template can be selectively removed and large areas containing tubular or fibers structures of polymer can be achieved. This is a simple procedure to produce fibers of conjugated polymer in films with enhanced optical and electrical properties that allows their application in optoelectronic devices.

  4. Polymer coating of glass microballoons levitated in a focused acoustic field

    NASA Technical Reports Server (NTRS)

    Young, A. T.; Lee, M. C.; Feng, I.-A.; Elleman, D. D.; Wang, T. G.

    1982-01-01

    Inertial confinement fusion (ICF) glass microballoons (GMBs) levitated in a focusing radiator acoustic device can be coated with liquid materials by deploying the liquid into the levitation field with a stepped-horn atomizer. The GMB can be forced to the center of the coating liquid with a strong acoustically generated centering force. Water solutions of organic polymers, UV-curable liquid organic monomers, and paraffin waxes have been used to prepare solid coatings on the surface of GMBs using this technique.

  5. Salt-Driven Deposition of Thermoresponsive Polymer-Coated Metal Nanoparticles on Solid Substrates.

    PubMed

    Zhang, Zhiyue; Maji, Samarendra; da Fonseca Antunes, André B; De Rycke, Riet; Hoogenboom, Richard; De Geest, Bruno G

    2016-06-13

    Here we report on a simple, generally applicable method for depositing metal nanoparticles on a wide variety of solid surfaces under all aqueous conditions. Noble-metal nanoparticles obtained by citrate reduction followed by coating with thermoresponsive polymers spontaneously form a monolayer-like structure on a wide variety of substrates in presence of sodium chloride whereas this phenomenon does not occur in salt-free medium. Interestingly, this phenomenon occurs below the cloud point temperature of the polymers and we hypothesize that salt ion-induced screening of electrostatic charges on the nanoparticle surface entropically favors hydrophobic association between the polymer-coated nanoparticles and a hydrophobic substrate. PMID:27142455

  6. Preparation and in-vitro Antibacterial Evaluation of Electroless Silver Coated Polymers

    PubMed Central

    Fazeli, Mohammad Reza; Hosseini, Vahid; Shamsa, Fazel; Jamalifar, Hossein

    2010-01-01

    Long-term use of indwelling medical catheters has often been hindered by catheter-associated nosocomial infections. In this study the effectiveness of silver coating of polystyrene and polyethylene polymers was investigated. Polymer pieces of 2 cm2 each were coated with a thin layer of silver using electroless plating technique. Silver-coated polymers were challenged with cultures of four different microorganisms known for their involvement in nosocomial infections in both solid and broth media. The tested bacteria included Staphylococcus aureus, Staphylococcus epidermidis, Escherichia coli and Pseudomonas aeruginosa. Silver release from the coated polymers was 2-5 μg/cm2 which was confirmed by chemical and biological methods. The silver coating thickness ranged between 20-450 nm. P. aeruginosa and S. aureus were the most adherent bacteria to polystyrene sheets while E. coli showed minimum adherence effect. The survival rate of different bacteria after 80 min in a time course experiment tended to dominate E. coli as the most sensitive bacteria to the effect of silver with zero survival rate while around 4% of P. aeruginosa were detected after same period. Silver coating of indwelling polymers by electroless technique seems promising in combating nosocomial infections due to long-term catheterization. PMID:24363735

  7. Electrochemical characterization of plasma polymer coatings in corrosion protection of aluminum alloys

    NASA Astrophysics Data System (ADS)

    Chan, Yenfong; Yu, Qingsong

    2005-07-01

    Low-temperature plasma polymerization is a promising pretreatment technique to create environmentally friendly coating systems for corrosion protection of aluminum alloys. In this study, the pretreatment effects of plasma treatment and plasma polymerization on corrosion properties of alclad aluminum alloy 2024-T3 ([2A]) were investigated using electrochemical characterization techniques, including cyclic polarization (CP) and electrochemical impedance spectroscopy (EIS). The [2A] panels were coated with an ultrathin layer (~50 nm) of plasma polymers in a direct current (dc) glow discharge of trimethylsilane or its mixtures with one of two diatomic gases (O2 and N2). The CP measurement results showed that the plasma polymer coated [2A] panels exhibited more negative corrosion potentials (Ecorr), smaller corrosion currents (Icorr), and no surface passivation when compared with uncoated [2A] control panels. The lower values of Icorr imply a higher corrosion resistance on the plasma polymer coated [2A]. When investigated using EIS, these plasma polymer coated [2A] panels exhibited higher impedance (|Z|) at lower frequency when first immersed in electrolyte solution, yet degraded quickly to a similar level as uncoated controls within 1 day of immersion. These results illustrated that thin plasma polymer films provided a certain but very limited corrosion resistance to [2A] substrate; their dominant role in plasma interface engineered coating systems still relied mostly on their adhesion enhancement at metal/paint interface as observed in our previous studies.

  8. Preparation and in-vitro Antibacterial Evaluation of Electroless Silver Coated Polymers.

    PubMed

    Fazeli, Mohammad Reza; Hosseini, Vahid; Shamsa, Fazel; Jamalifar, Hossein

    2010-01-01

    Long-term use of indwelling medical catheters has often been hindered by catheter-associated nosocomial infections. In this study the effectiveness of silver coating of polystyrene and polyethylene polymers was investigated. Polymer pieces of 2 cm(2) each were coated with a thin layer of silver using electroless plating technique. Silver-coated polymers were challenged with cultures of four different microorganisms known for their involvement in nosocomial infections in both solid and broth media. The tested bacteria included Staphylococcus aureus, Staphylococcus epidermidis, Escherichia coli and Pseudomonas aeruginosa. Silver release from the coated polymers was 2-5 μg/cm(2) which was confirmed by chemical and biological methods. The silver coating thickness ranged between 20-450 nm. P. aeruginosa and S. aureus were the most adherent bacteria to polystyrene sheets while E. coli showed minimum adherence effect. The survival rate of different bacteria after 80 min in a time course experiment tended to dominate E. coli as the most sensitive bacteria to the effect of silver with zero survival rate while around 4% of P. aeruginosa were detected after same period. Silver coating of indwelling polymers by electroless technique seems promising in combating nosocomial infections due to long-term catheterization. PMID:24363735

  9. Cotton Fabric Coated with Conducting Polymers and its Application in Monitoring of Carnivorous Plant Response.

    PubMed

    Bajgar, Václav; Penhaker, Marek; Martinková, Lenka; Pavlovič, Andrej; Bober, Patrycja; Trchová, Miroslava; Stejskal, Jaroslav

    2016-01-01

    The paper describes the electrical plant response to mechanical stimulation monitored with the help of conducting polymers deposited on cotton fabric. Cotton fabric was coated with conducting polymers, polyaniline or polypyrrole, in situ during the oxidation of respective monomers in aqueous medium. Thus, modified fabrics were again coated with polypyrrole or polyaniline, respectively, in order to investigate any synergetic effect between both polymers with respect to conductivity and its stability during repeated dry cleaning. The coating was confirmed by infrared spectroscopy. The resulting fabrics have been used as electrodes to collect the electrical response to the stimulation of a Venus flytrap plant. This is a paradigm of the use of conducting polymers in monitoring of plant neurobiology. PMID:27070612

  10. Cotton Fabric Coated with Conducting Polymers and its Application in Monitoring of Carnivorous Plant Response

    PubMed Central

    Bajgar, Václav; Penhaker, Marek; Martinková, Lenka; Pavlovič, Andrej; Bober, Patrycja; Trchová, Miroslava; Stejskal, Jaroslav

    2016-01-01

    The paper describes the electrical plant response to mechanical stimulation monitored with the help of conducting polymers deposited on cotton fabric. Cotton fabric was coated with conducting polymers, polyaniline or polypyrrole, in situ during the oxidation of respective monomers in aqueous medium. Thus, modified fabrics were again coated with polypyrrole or polyaniline, respectively, in order to investigate any synergetic effect between both polymers with respect to conductivity and its stability during repeated dry cleaning. The coating was confirmed by infrared spectroscopy. The resulting fabrics have been used as electrodes to collect the electrical response to the stimulation of a Venus flytrap plant. This is a paradigm of the use of conducting polymers in monitoring of plant neurobiology. PMID:27070612

  11. Effect of soluble polymer binder on particle distribution in a drying particulate coating.

    PubMed

    Buss, Felix; Roberts, Christine C; Crawford, Kathleen S; Peters, Katharina; Francis, Lorraine F

    2011-07-01

    Soluble polymer is frequently added to inorganic particle suspensions to provide mechanical strength and adhesiveness to particulate coatings. To engineer coating microstructure, it is essential to understand how drying conditions and dispersion composition influence particle and polymer distribution in a drying coating. Here, a 1D model revealing the transient concentration profiles of particles and soluble polymer in a drying suspension is proposed. Sedimentation, evaporation and diffusion govern particle movement with the presence of soluble polymer influencing the evaporation rate and solution viscosity. Results are summarized in drying regime maps that predict particle accumulation at the free surface or near the substrate as conditions vary. Calculations and experiments based on a model system of poly(vinyl alcohol) (PVA), silica particles and water reveal that the addition of PVA slows the sedimentation and diffusion of the particles during drying such that accumulation of particles at the free surface is more likely. PMID:21497825

  12. Study on iron oxide nanoparticles coated with glucose-derived polymers for biomedical applications

    NASA Astrophysics Data System (ADS)

    Herea, D. D.; Chiriac, H.; Lupu, N.; Grigoras, M.; Stoian, G.; Stoica, B. A.; Petreus, T.

    2015-10-01

    This study reports an approach for a facile one-step synthesis of magnetic nanoparticles (MNPs) coated with glucose-derived polymers (GDP) through a mechanochemical hydrothermal process for biomedical applications. Polymer-coated magnetic nanoparticles (Fe2O3/Fe3O4), with sizes below 10 nm, exhibited superparamagnetic behavior, with a specific magnetization saturation value of about 40 emu/g, and a maximum specific absorption rate (SAR) of 30 W/g in AC magnetic fields. Depending on the intensity of the applied AC magnetic field, a temperature of 42 °C can be achieved in 4-17 min. The surface polymerized layer affords functional hydroxyl groups for binding to biomolecules containing carboxyl, thiol, or amino groups, thereby making the coated nanoparticles feasible for bio-conjugation. In vitro cytotoxicity evaluation pointed out that a relatively high concentration of polymer-coated magnetic nanoparticles (GDP-MNPs) did not induce severe cell alteration, suggesting a good biocompatibility.

  13. Conducting polymer/polyimide-clay nanocomposite coatings for corrosion protection of AA-2024 alloy

    NASA Astrophysics Data System (ADS)

    Shah, Kunal G.

    Corrosion of metals is a major problem in the aerospace and automobile industry. The current methods of corrosion protection such as chromate conversion coatings are under increased scrutiny from the Environmental Protection Agency (EPA) due to their carcinogenic nature. Intrinsically conducting polymers (ICPs) like polyaniline and polypyrrole have been considered as a potential replacement for chromate conversion coatings and have been under investigation since past decade. The goal of this study is to replace the chromate conversion coating by an environmentally friendly organic coating. Poly (N-ethyl aniline) coating was electrodeposited as the primer layer and polyimide-clay nanocomposite was solution cast as the barrier layer on AA-2024 alloy. This study will provide a better understanding of the corrosion protection mechanism of the conducting polymer coating. Various characterization techniques such as infrared spectroscopy, cyclic voltammetry and scanning electron microscopy were used to study the formation, chemical structure and morphology of the coatings. Electrodeposition parameters like monomer concentration, applied current density and the reaction time were varied in order to optimize the properties of the conducting polymer coating. The corrosion performance of the primer coating was evaluated by DC polarization studies. It was found that poly (N-ethyl aniline) reduces from emeraldine to leucoemeraldine form; reducing the rate of cathodic reaction, which reduces the rate of corrosion of AA-2024 alloy. Polyimide-clay nanocomposite coating was solution cast on the conducting polymer primer layer for enhancing the barrier and corrosion properties of the coating system. The concentration of polyimide (10--25 vol%) and clay (0.1 and 1 wt%) were varied in the coating formulation to optimize the barrier properties of topcoat. X-ray diffraction showed that the intergallery clay distance decreased from 17.2 A to 11.79 A after immidization of polyimide

  14. In vitro antimicrobial properties of silver-polysaccharide coatings on porous fiber-reinforced composites for bone implants.

    PubMed

    Nganga, Sara; Travan, Andrea; Marsich, Eleonora; Donati, Ivan; Söderling, Eva; Moritz, Niko; Paoletti, Sergio; Vallittu, Pekka K

    2013-12-01

    Biostable fiber-reinforced composite (FRC) implants prepared from bisphenol-A-dimethacrylate and triethyleneglycoldimethacrylate resin reinforced with E-glass fibers have been successfully used in cranial reconstructions in 15 patients. Recently, porous FRC structures were suggested as potential implant materials. Compared with smooth surface, porous surface allows implant incorporation via bone ingrowth, but is also a subject to bacterial attachment. Non-cytotoxic silver-polysaccharide nanocomposite coatings may provide a way to decrease the risk of bacterial contamination of porous FRC structures. This study is focused on the in vitro characterization of the effect porosity on the antimicrobial efficiency of the coatings against Staphylococcus aureus and Pseudomonas aeruginosa by a series of microbiological tests (initial adhesion, antimicrobial efficacy, and biofilm formation). Characterization included confocal laser scanning microscopy and scanning electron microscopy. The effect of porosity on the initial attachment of S. aureus was pronounced, but in the case of P. aeruginosa the effect was negligible. There were no significant effects of the coatings on the initial bacterial attachment. In the antimicrobial efficacy test, the coatings were potent against both strains regardless of the sample morphology. In the biofilm tests, there were no clear effects either of morphology or of the coating. Further coating development is foreseen to achieve a longer-term antimicrobial effect to inhibiting bacterial implant colonization. PMID:23922117

  15. Localized cell stimulation by nitric oxide using a photoactive porous coordination polymer platform

    NASA Astrophysics Data System (ADS)

    Diring, Stéphane; Wang, Dan Ohtan; Kim, Chiwon; Kondo, Mio; Chen, Yong; Kitagawa, Susumu; Kamei, Ken-Ichiro; Furukawa, Shuhei

    2013-10-01

    Functional cellular substrates for localized cell stimulation by small molecules provide an opportunity to control and monitor cell signalling networks chemically in time and space. However, despite improvements in the controlled delivery of bioactive compounds, the precise localization of gaseous biomolecules at the single-cell level remains challenging. Here we target nitric oxide, a crucial signalling molecule with site-specific and concentration-dependent activities, and we report a synthetic strategy for developing spatiotemporally controllable nitric oxide-releasing platforms based on photoactive porous coordination polymers. By organizing molecules with poor reactivity into polymer structures, we observe increased photoreactivity and adjustable release using light irradiation. We embed photoactive polymer crystals in a biocompatible matrix and achieve precisely controlled nitric oxide delivery at the cellular level via localized two-photon laser activation. The biological relevance of the exogenous nitric oxide produced by this strategy is evidenced by an intracellular change in calcium concentration, mediated by nitric oxide-responsive plasma membrane channel proteins.

  16. Permeability modification in 3D porous media due to polymer retention

    NASA Astrophysics Data System (ADS)

    Parsa, Shima; Sizaret, Hubert; Weitz, David

    2015-11-01

    We combine confocal microscopy and bulk transport measurements to quantify the changes in the permeability of a model porous media after flow of a polymer solution. The 3D micromodel is made of closely packed glass beads with diameter of 150 micrometers. By matching the index of refraction of the fluid with beads we are able to measure the fluid velocities at pore level deep in the medium using particle image velocimetry. Our measurement shows that the medium permeability decreases 60% after flow of multiple pore volumes of polymer solution and then flushing with water. At constant flow rate we estimate that the pore velocity increases almost 23% due to this reduction in permeability. Our microscopic measurements of the velocities in pores shows that the average velocity increases considerably more than estimated bulk value. Also the distribution of velocities has a slower decay indicating somewhat higher probability of large velocities in the medium after retention of polymer. These changes in velocities are not uniform and depends on the pore size.

  17. A computational study of bulk porous two-dimensional polymers related to graphyne.

    PubMed

    Sánchez-González, A; Dobado, J A; Torneiro, M

    2016-08-01

    Over the last twelve years there has been an explosion in the area of reticular chemistry with several classes of carbonaceous or carbon-rich reticular compounds coming into the scene and/or suffering an exponential growth in the number of related studies. Examples are MOFs, COFs, graphene and 2D polymers. π-Conjugated reticular compounds in particular are of great interest due to their optoelectronic properties. In this study we use density functional theory methods with periodic boundary conditions to investigate the stacking arrangements of bulk 2D polymer multilayer porous graphyne A, the related carbon allotrope multilayer graphyne B, and the analog bulk 2D polymer C in which the triple bonds of A are substituted by double bonds. The results show that for the three materials the eclipsed stacking arrangements are considerably less stable than staggered and slipped arrangements, with the more stable structures being slipped, staggered and off-centered-staggered arrangements for A, B and C, respectively. To shed light on the π-π interactions responsible for the geometry and relative energies of the different stacking modes we analyze the topology of the electron density using the electron localization function. In addition, simulated patterns for powder X-ray diffraction have been obtained from the optimized systems, which can be used for identification of the bulk 2D reticular compounds in future syntheses. PMID:27426443

  18. Rational Design of Porous Conjugated Polymers and Roles of Residual Palladium for Photocatalytic Hydrogen Production.

    PubMed

    Li, Lianwei; Cai, Zhengxu; Wu, Qinghe; Lo, Wai-Yip; Zhang, Na; Chen, Lin X; Yu, Luping

    2016-06-22

    Developing highly efficient photocatalyts for water splitting is one of the grand challenges in solar energy conversion. Here, we report the rational design and synthesis of porous conjugated polymer (PCP) that photocatalytically generates hydrogen from water splitting. The design mimics natural photosynthetics systems with conjugated polymer component to harvest photons and the transition metal part to facilitate catalytic activities. A series of PCPs have been synthesized with different light harvesting chromophores and transition metal binding bipyridyl (bpy) sites. The photocatalytic activity of these bpy-containing PCPs can be greatly enhanced due to the improved light absorption, better wettability, local ordering structure, and the improved charge separation process. The PCP made of strong and fully conjugated donor chromophore DBD (M4) shows the highest hydrogen production rate at ∼33 μmol/h. The results indicate that copolymerization between a strong electron donor and weak electron acceptor into the same polymer chain is a useful strategy for developing efficient photocatalysts. This study also reveals that the residual palladium in the PCP networks plays a key role for the catalytic performance. The hydrogen generation activity of PCP photocatalyst can be further enhanced to 164 μmol/h with an apparent quantum yield of 1.8% at 350 nm by loading 2 wt % of extra platinum cocatalyst. PMID:27254306

  19. Thermomechanical analysis and durability of commercial micro-porous polymer Li-ion battery separators

    NASA Astrophysics Data System (ADS)

    Love, Corey T.

    2011-03-01

    Static and dynamic thermomechanical analysis was performed with a dynamic mechanical analyzer (DMA) to identify thermal and mechanical transitions for commercially available polymer separators under mechanical loading. Clear transitions in deformation mode were observed at elevated temperatures. These transitions identified the onset of separator "shutdown" which occurred at temperatures below the polymer melting point. Mechanical loading direction was critical to the overall integrity of the separator. Anisotropic separators (Celgard 2320, 2400 and 2500) were mechanically limited when pulled in tensile in the transverse direction. The anisotropy of these separators is a result of the dry technique used to manufacture the micro-porous membranes. Separators prepared using the wet technique (Entek Gold LP) behaved more uniformly, or biaxially, where all mechanical properties were nearly identical within the separator plane. The information provided by the DMA can also be useful for predicting the long-term durability of polymer separators in lithium-ion batteries exposed to electrolyte (solvent and salt), thermal fluctuations and electrochemical cycling. Small losses in mechanical integrity were observed for separators exposed to the various immersion environments over the 4-week immersion time.

  20. Localized cell stimulation by nitric oxide using a photoactive porous coordination polymer platform

    PubMed Central

    Diring, Stéphane; Wang, Dan Ohtan; Kim, Chiwon; Kondo, Mio; Chen, Yong; Kitagawa, Susumu; Kamei, Ken-ichiro; Furukawa, Shuhei

    2013-01-01

    Functional cellular substrates for localized cell stimulation by small molecules provide an opportunity to control and monitor cell signalling networks chemically in time and space. However, despite improvements in the controlled delivery of bioactive compounds, the precise localization of gaseous biomolecules at the single-cell level remains challenging. Here we target nitric oxide, a crucial signalling molecule with site-specific and concentration-dependent activities, and we report a synthetic strategy for developing spatiotemporally controllable nitric oxide-releasing platforms based on photoactive porous coordination polymers. By organizing molecules with poor reactivity into polymer structures, we observe increased photoreactivity and adjustable release using light irradiation. We embed photoactive polymer crystals in a biocompatible matrix and achieve precisely controlled nitric oxide delivery at the cellular level via localized two-photon laser activation. The biological relevance of the exogenous nitric oxide produced by this strategy is evidenced by an intracellular change in calcium concentration, mediated by nitric oxide-responsive plasma membrane channel proteins. PMID:24158008

  1. Development of Porous YSZ Coatings with Modified Thermal and Optical Properties by Plasma Spray Physical Vapor Deposition

    NASA Astrophysics Data System (ADS)

    Kambara, Makoto; Shinozawa, Akihiro; Aoshika, Kiyoshi; Eguchi, Keisuke; Yoshida, Toyonobu

    Porous and feather-like yttria-stabilized zirconia coatings have been deposited by plasma spray physical vapor deposition (PS-PVD) at the deposition rate of around 200 µm/min. The porosity of the coating reached > 50% and the overall thermal conductivity was reduced less than 0.5 W/mK, both of which were fundamentally independent of the coating thickness up to 120 µm. Such coating structures were characterized by their high scattering coefficients at light wavelength from 2 to 6 µm, and thus the transmittance to infrared was reduced significantly compared to the splat structure coating with the identical thickness. The thermal properties of these coatings were retained even after annealing at temperature ˜1500°C for 130 hours.

  2. Image measurements of unsteady pressure fluctuation by a pressure-sensitive coating on porous anodized aluminium

    NASA Astrophysics Data System (ADS)

    Kameda, M.; Tabei, T.; Nakakita, K.; Sakaue, H.; Asai, K.

    2005-12-01

    Pressure-sensitive luminescent coating on porous anodized aluminium (AA-PSP) was applied to measure non-periodic unsteady pressure distribution on a wind-tunnel model. A high-speed digital video camera was used to capture the PSP signal. The pressure-sensitive dye was tris(4,7-diphenylphenanthroline) ruthenium(II) ([Ru(dpp)3]2+). The coating has a short response time of O(10 µs), although it exhibits temperature and humidity sensitivities. A hydrophobic coating was applied on the anodized aluminium surface to suppress the humidity sensitivity. A temperature sensitive paint was used to obtain the temperature distribution instantaneously with the pressure. The temperature data were used to correct the PSP response. An appropriate data acquisition procedure as well as digital image processing algorithm was established to compensate for the error from the temperature and humidity sensitivities. The present system was applied to measure the pressure distribution on a delta wing at a high angle of attack in transonic flow, whose flow is unsteady due to the interaction between shock waves and leading edge vortices. The non-periodic unsteady pressure distribution on the delta wing was successfully measured with the sampling rate of 1 kHz and within a few per cent error in absolute pressure level.

  3. Porous-coated acetabular components with screw fixation. Five to ten-year results.

    PubMed

    Latimer, H A; Lachiewicz, P F

    1996-07-01

    The results of 136 consecutive primary total hip arthroplasties performed by one surgeon with the Harris-Galante-I porous-coated acetabular component were reviewed at a mean of seven years (range, five to ten years). In all hips, the outer diameter of the acetabular component was the same as the diameter of the final reamer used in the preparation of the acetabulum. However, this reamer was used only briefly at the rim of the acetabulum, and therefore the components had so-called press-fit stability. A mean of four screws (range, three to six screws) were used for additional fixation of the component. The clinical evaluation was performed with use of the Harris hip score. Standardized anteroposterior radiographs of the pelvis were assessed for migration of the component, radiolucent and radiodense lines, linear wear of the polyethylene, and osteolysis. No acetabular component had been revised for loosening and none were radiographically loose at the time of the most recent follow-up evaluation. There were no complications related to the use of the screws, and no screw had bent or broken. A non-progressive radiolucent line was seen in one acetabular zone in thirty-four hips (25 per cent) and in two acetabular zones in six hips (4 per cent). No hip had a radiolucent line in all three acetabular zones. The mean rate of linear wear of the polyethylene was 0.1 millimeter per year. There was no dissociation of the acetabular liner from the metal shell. Two hips (1 per cent) had asymptomatic osteolysis in the ischium and adjacent to the rim of the acetabular component; this was treated with grafting at the site of the lesion and exchange of the femoral head and the worn polyethylene liner. Five femoral components inserted without cement and one inserted with cement were revised because of loosening. The data suggest that, at a mean of seven years, fixation of this porous-coated component was uniformly excellent. The low prevalence of radiolucent lines and the absence of

  4. Semi-permeable coatings fabricated from comb-polymers efficiently protect proteins in vivo.

    PubMed

    Liu, Mi; Johansen, Pål; Zabel, Franziska; Leroux, Jean-Christophe; Gauthier, Marc A

    2014-01-01

    In comparison to neutral linear polymers, functional and architecturally complex (that is, non-linear) polymers offer distinct opportunities for enhancing the properties and performance of therapeutic proteins. However, understanding how to harness these parameters is challenging, and studies that capitalize on them in vivo are scarce. Here we present an in vivo demonstration that modification of a protein with a polymer of appropriate architecture can impart low immunogenicity, with a commensurably low loss of therapeutic activity. These combined properties are inaccessible by conventional strategies using linear polymers. For the model protein L-asparaginase, a comb-polymer bio-conjugate significantly outperformed the linear polymer control in terms of lower immune response and more sustained bioactivity. The semi-permeability characteristics of the coatings are consistent with the phase diagram of the polymer, which will facilitate the application of this strategy to other proteins and with other therapeutic models. PMID:25407758

  5. Piezoelectric biosensor with a ladder polymer substrate coating

    DOEpatents

    Renschler, C.L.; White, C.A.; Carter, R.M.

    1998-09-29

    A piezoelectric biosensor substrate useful for immobilizing biomolecules in an oriented manner on the surface of a piezoelectric sensor has a ladder polymer of polyacrylonitrile. To make the substrate, a solution of an organic polymer, preferably polyacrylonitrile, is applied to the surface of a piezoelectric sensor. The organic polymer is modifying by heating the polymer in a controlled fashion in air such that a ladder polymer is produced which, in turn, forms the attachment point for the biomolecules comprising the piezoelectric biosensor. 3 figs.

  6. Use of a self-assembling organogel as a reverse template in the preparation of imprinted porous polymer films.

    PubMed

    Tan, Grace; Singh, Mohit; He, Jibao; John, Vijay T; McPherson, Gary L

    2005-09-27

    The concept of reverse templating of an organogel to form imprinted porous divinylbenzene polymer films with submicrometer channels is demonstrated. The organogel comprising a 1:1 molar ratio of two organogelators, that is, bis(2-ethylhexyl) sodium sulfosuccinate and 4-chlorophenol, was formed in divinylbenzene. The gel was cast as a thin film before UV polymerization of the solvent, and the organogelators were later removed by simple washing with water and isooctane. The integrity of the fiber bundles of the organogel was preserved during polymerization, and an exact hollow replica was obtained after the organogelators were leached away. It is easily possible to imprint gel fiber bundle structures into polymeric films through this technique. The gel can also be formed on macroporous substrates to yield supported thin porous polymeric films. With the incorporation of functional nanoparticles in AOT inverse micelles and hence the organogel, nanoparticle-containing porous polymer films exhibiting luminescence or magnetic properties are envisioned. PMID:16171368

  7. Porous silica coated spherical microresonator for vapor phase sensing of ammonia at a sub-ppm level

    NASA Astrophysics Data System (ADS)

    Mallik, Arun K.; Farrell, Gerald; Liu, Dejun; Kavungal, Vishnu; Wu, Qiang; Semenova, Yuliya

    2016-05-01

    A new type of fiber optic sensor for the detection and quantification of ammonia (NH3) vapor levels is proposed and experimentally demonstrated. This sensor is based on a spherical silica micro resonator coated with porous silica gel. Whispering gallery modes (WGMs) in the micro resonator are excited by evanescent coupling to a tapered fiber with a 3.3 μm waist diameter. The optical properties of the porous silica layer change when it is exposed to ammonia vapor, leading to a spectral shift of the WGM resonant wavelengths. The sensitivity of the proposed sensor has been tested by exposing it to different low level concentrations of ammonia: 4 ppm, 8 ppm, 12 ppm and 30 ppm at a constant relative humidity (50% RH) and constant temperature (23°C). The detection limit is calculated from experimental results as 57 ppb of ammonia for a 282 μm diameter porous silica coated microsphere.

  8. Coating of meso-porous metallic membranes with oriented channel-like fine pores by pulsed laser deposition.

    PubMed

    Mukherji, D; Lackner, J; Wanderka, N; Kardjilov, N; Näth, O; Jäger, S; Schmitz, F; Rösler, J

    2008-02-13

    There is increasing demand to functionalize meso- and nanoporous materials by coating and make the porous substrate biocompatible or environmentally friendly. However, coating on a meso-porous substrate poses great challenges, especially if the pore aspect ratio is high. We adopted the pulsed laser deposition (PLD) method to coat Ni(3)Al-based meso-porous membranes, which were fabricated from a single-crystal Ni-based superalloy by a unique selective phase dissolution technique. These membranes were about 250 µm thick and had channel-like pores (∼200 nm wide) with very high aspect ratio. Two different coating materials, i.e. diamond-like carbon (DLC) and titanium, were used to coat these membranes. High energy C or Ti ions, produced in the plasma plume by the PLD process, penetrated the channel-like pores and deposited coatings on the pore walls deep inside the membrane. The thickness and the quality of coatings on the pore walls were examined using the dual-beam system. The coating thickness, of the order of 50 nm, was adherent to the pore walls and was quite uniform at different depths. The carbon and the Ti deposition behaved quite similarly. The preliminary experiments showed that the PLD is an adequate method for coating fine open cavities of complex geometry. Simulations based on stopping and the range of ions in matter (SRIM) calculations helped in understanding the deposition processes on pore walls at great depths. PMID:21730712

  9. Self-healing antimicrobial polymer coating with efficacy in the presence of organic matter

    NASA Astrophysics Data System (ADS)

    Bastarrachea, Luis J.; Goddard, Julie M.

    2016-08-01

    A method to prepare a self-healing, antimicrobial polymer coating that retains efficacy against Escherichia coli O157:H7 in the presence of organic matter is reported. A coating composed of branched polyethyleneimine (PEI) and styrene maleic anhydride copolymer (SMA) was applied to a maleic anhydride functionalized polypropylene support. The chemistry of the polymer coating was designed to impart hydrophobicity due to the styrene subunits, intrinsic antimicrobial character (>99.9% reduction) from the cationic primary amine groups, and enhanced antimicrobial character (> 99.99% reduction) after chlorination of N-halamine forming groups. Antimicrobial effectiveness was demonstrated under conditions of increasing organic load. Up to 500 ppm horse serum, chlorinated coatings retained full antimicrobial character (>99.99% reduction). Even at 50,000 ppm of horse serum, the coating provided ∼90% reduction as prepared, and between ∼75% and ∼80% reduction in the form of N-halamines. Microscopy confirmed no evidence of bacterial adhesion on the coating surface. Finally, the coating exhibited self-healing properties after exposure to acid and alkaline solutions and restoration by heat, as confirmed through spectroscopy from the rebuilding of characteristic chemical bonds. Such robust antimicrobial polymer coatings with efficacy under conditions of increasing organic load may support reducing microbial cross-contamination in food and biomedical industries.

  10. Porous polymers bearing functional quaternary ammonium salts as efficient solid catalysts for the fixation of CO2 into cyclic carbonates

    NASA Astrophysics Data System (ADS)

    Cai, Sheng; Zhu, Dongliang; Zou, Yan; Zhao, Jing

    2016-07-01

    A series of porous polymers bearing functional quaternary ammonium salts were solvothermally synthesized through the free radical copolymerization of divinylbenzene (DVB) and functionalized quaternary ammonium salts. The obtained polymers feature highly cross-linked matrices, large surface areas, and abundant halogen anions. These polymers were evaluated as heterogeneous catalysts for the synthesis of cyclic carbonates from epoxides and CO2 in the absence of co-catalysts and solvents. The results revealed that the synergistic effect between the functional hydroxyl groups and the halide anion Br- afforded excellent catalytic activity to cyclic carbonates. In addition, the catalyst can be easily recovered and reused for at least five cycles without significant loss in activity.

  11. Modeling of Multiphase Flow through Thin Porous Layers: Application to a Polymer Electrolyte Fuel Cell (PEFC)

    NASA Astrophysics Data System (ADS)

    Qin, C.; Hassanizadeh, S.

    2013-12-01

    Multiphase flow and species transport though thin porous layers are encountered in a number of industrial applications, such as fuel cells, filters, and hygiene products. Based on some macroscale models like the Darcy's law, to date, the modeling of flow and transport through such thin layers has been mostly performed in 3D discretized domains with many computational cells. But, there are a number of problems with this approach. First, a proper representative elementary volume (REV) is not defined. Second, one needs to discretize a thin porous medium into computational cells whose size may be comparable to the pore sizes. This suggests that the traditional models are not applicable to such thin domains. Third, the interfacial conditions between neighboring layers are usually not well defined. Last, 3D modeling of a number of interacting thin porous layers often requires heavy computational efforts. So, to eliminate the drawbacks mentioned above, we propose a new approach to modeling multilayers of thin porous media as 2D interacting continua (see Fig. 1). Macroscale 2D governing equations are formulated in terms of thickness-averaged material properties. Also, the exchange of thermodynamic properties between neighboring layers is described by thickness-averaged quantities. In Comparison to previous macroscale models, our model has the distinctive advantages of: (1) it is rigorous thermodynamics-based model; (2) it is formulated in terms of thickness-averaged material properties which are easily measureable; and (3) it reduces 3D modeling to 2D leading to a very significant reduction of computation efforts. As an application, we employ the new approach in the study of liquid water flooding in the cathode of a polymer electrolyte fuel cell (PEFC). To highlight the advantages of the present model, we compare the results of water distribution with those obtained from the traditional 3D Darcy-based modeling. Finally, it is worth noting that, for specific case studies, a

  12. Facile Carbonization of Microporous Organic Polymers into Hierarchically Porous Carbons Targeted for Effective CO2 Uptake at Low Pressures.

    PubMed

    Gu, Shuai; He, Jianqiao; Zhu, Yunlong; Wang, Zhiqiang; Chen, Dongyang; Yu, Guipeng; Pan, Chunyue; Guan, Jianguo; Tao, Kai

    2016-07-20

    The advent of microporous organic polymers (MOPs) has delivered great potential in gas storage and separation (CCS). However, the presence of only micropores in these polymers often imposes diffusion limitations, which has resulted in the low utilization of MOPs in CCS. Herein, facile chemical activation of the single microporous organic polymers (MOPs) resulted in a series of hierarchically porous carbons with hierarchically meso-microporous structures and high CO2 uptake capacities at low pressures. The MOPs precursors (termed as MOP-7-10) with a simple narrow micropore structure obtained in this work possess moderate apparent BET surface areas ranging from 479 to 819 m(2) g(-1). By comparing different activating agents for the carbonization of these MOPs matrials, we found the optimized carbon matrials MOPs-C activated by KOH show unique hierarchically porous structures with a significant expansion of dominant pore size from micropores to mesopores, whereas their microporosity is also significantly improved, which was evidenced by a significant increase in the micropore volume (from 0.27 to 0.68 cm(3) g(-1)). This maybe related to the collapse and the structural rearrangement of the polymer farmeworks resulted from the activation of the activating agent KOH at high temperature. The as-made hierarchically porous carbons MOPs-C show an obvious increase in the BET surface area (from 819 to 1824 m(2) g(-1)). And the unique hierarchically porous structures of MOPs-C significantly contributed to the enhancement of the CO2 capture capacities, which are up to 214 mg g(-1) (at 273 K and 1 bar) and 52 mg g(-1) (at 273 K and 0.15 bar), superior to those of the most known MOPs and porous carbons. The high physicochemical stabilities and appropriate isosteric adsorption heats as well as high CO2/N2 ideal selectivities endow these hierarchically porous carbon materials great potential in gas sorption and separation. PMID:27332739

  13. Polymer-Derived Ceramics as Innovative Oxidation Barrier Coatings for Mo-Si-B Alloys

    NASA Astrophysics Data System (ADS)

    Hasemann, Georg; Baumann, Torben; Dieck, Sebastian; Rannabauer, Stefan; Krüger, Manja

    2015-04-01

    A preceramic polymer precursor, perhydropolysilazane, is used to investigate its function as a new type of oxidation barrier coating on Mo-Si-B alloys. After dip-coating and pyrolysis at 1073 K (800 °C), dense and well-adhering SiON ceramic coatings could be achieved, which were investigated by SEM and cyclic oxidation tests at 1073 K and 1373 K (800 °C and 1100 °C). The coating is promising in reducing the mass loss during the initial stage of oxidation exposure at 1373 K (1100 °C) significantly.

  14. Void space modeling of mercury intrusion hysteresis in sandstone, paper coating, and other porous media

    SciTech Connect

    Matthews, G.P.; Ridgway, C.J.; Spearing, M.C.

    1995-04-01

    A void space network is presented for the simulation of mercury intrusion hysteresis in outcrop and reservoir sandstones and paper coatings. Three methods are described which allow the convergence of the simulation onto experiment, each finding the optimum pore and throat size distributions and connectivity according to different criteria. The simulated pore and throat size distributions are entirely different from the first derivatives of the intrusion curves which are commonly employed. The optimum void space networks, which have the correct porosity, are then used to simulate the hysteresis which occurs when the mercury is withdrawn. The effects of contact angle hysteresis and trapping within wide pores adjacent to narrow throats are demonstrated. Considerable trapping of mercury is found to occur because of snap-off effects, without invoking any dead-end pores. Similar networks have been used to simulate absolute gas permeability, tortuosity, diffusion, formation factor, and colloidal flow formation damage and can be applied to any porous medium.

  15. Uncemented acetabular components. Histologic analysis of retrieved hydroxyapatite-coated and porous implants.

    PubMed

    Bauer, T W; Stulberg, B N; Ming, J; Geesink, R G

    1993-04-01

    Histologic sections of five hydroxyapatite-coated acetabular components retrieved at autopsy (2 dual geometry and 3 threaded cup designs) were analyzed, and the extent and pattern of bone apposition were compared with that of an uncoated, porous (beaded) dual geometry acetabular cup that had been removed for repeated dislocations. The results show hydroxyapatite and bone apposition most prominent in areas of likely load transmission, primarily around the peripheral rim of the dual-geometry cups and at the peaks of the threads of the screw cups. Hydroxyapatite and bone may have been removed by remodeling from the grooves between the threads. Although no significant wear debris was identified, the screw holes were incompletely covered by bone. The dual-geometry designs generally showed somewhat more bone apposition than the threaded cups, but all implants demonstrated less bone than might have been predicted from radiographs. PMID:8386747

  16. Ex Situ Integration of Multifunctional Porous Polymer Monoliths into Thermoplastic Microfluidic Chips

    PubMed Central

    Kendall, Eric L.; Wienhold, Erik; Rahmanian, Omid D.; DeVoe, Don L.

    2014-01-01

    A unique method for incorporating functional porous polymer monolith elements into thermoplastic microfluidic chips is described. Monolith elements are formed in a microfabricated mold, rather than within the microchannels, and chemically functionalized off chip before insertion into solvent-softened thermoplastic microchannels during chip assembly. Because monoliths may be trimmed prior to final placement, control of their size, shape, and uniformity is greatly improved over in-situ photopolymerization methods. A characteristic trapezoidal profile facilitates rapid insertion and enables complete mechanical anchoring of the monolith periphery, eliminating the need for chemical attachment to the microchannel walls. Off-chip processing allows the parallel preparation of monoliths of differing compositions and surface chemistries in large batches. Multifunctional flow-through arrays of multiple monolith elements are demonstrated using this approach through the creation of a fluorescent immunosensor with integrated controls, and a microfluidic bubble separator comprising a combination of integrated hydrophobic and hydrophilic monolith elements. PMID:25018587

  17. High internal phase emulsion templating--a path to hierarchically porous functional polymers.

    PubMed

    Pulko, Irena; Krajnc, Peter

    2012-10-26

    Recently, a series of new monomers and polymerization mechanisms has been applied to the templating of high internal phase emulsions (HIPEs) providing a route to hierarchically porous materials with a range of functionalities and applications. The high degree of control over the pore size is another attractive feature of these materials. Usually, the continuous phase contains monomers, the droplet phase is used to template the large, primary pores, which are interconnected by secondary pores. The addition of nonpolymerizable components to the continuous phase can result in phase separation during polymerization and tertiary pores. Applications include polymer supports for catalysis and synthesis, separation and filtration, cell culture media, enzyme supports, and structural and isolation applications. PMID:22907672

  18. Catalytic glucose isomerization by porous coordination polymers with open metal sites.

    PubMed

    Akiyama, George; Matsuda, Ryotaro; Sato, Hiroshi; Kitagawa, Susumu

    2014-10-01

    Highly efficient catalytic isomerization reactions from glucose to fructose in aqueous media using porous coordination polymers (PCPs) or metal-organic frameworks (MOFs) is reported for the first time. The catalytic activity of PCPs functionalized with -NH2, -(CH3)2, -NO2, and -SO3H groups on the pore surface is systematically tested. The catalytic activity can be tuned by the acidity of open metal sites (OMSs) by modifying the organic linkers with the functional groups. As a result, it is demonstrated that MIL-101 functionalized with -SO3H not only shows high conversion of glucose but also selectively produces fructose. Further, catalytic one-pot conversion of amylose to fructose is achieved, thanks to the high stability of the framework in an acidic solution. These results show that MOF/PCP compounds having OMSs are promising materials for various useful heterogeneous catalytic reactions, in particular in the biomass field. PMID:25080129

  19. Control of molecular rotor rotational frequencies in porous coordination polymers using a solid-solution approach.

    PubMed

    Inukai, Munehiro; Fukushima, Tomohiro; Hijikata, Yuh; Ogiwara, Naoki; Horike, Satoshi; Kitagawa, Susumu

    2015-09-30

    Rational design to control the dynamics of molecular rotors in crystalline solids is of interest because it offers advanced materials with precisely tuned functionality. Herein, we describe the control of the rotational frequency of rotors in flexible porous coordination polymers (PCPs) using a solid-solution approach. Solid-solutions of the flexible PCPs [{Zn(5-nitroisophthalate)x(5-methoxyisophthalate)1-x(deuterated 4,4'-bipyridyl)}(DMF·MeOH)]n allow continuous modulation of cell volume by changing the solid-solution ratio x. Variation of the isostructures provides continuous changes in the local environment around the molecular rotors (pyridyl rings of the 4,4'-bipyridyl group), leading to the control of the rotational frequency without the need to vary the temperature. PMID:26368067

  20. Multi-length scale porous polymer films from hypercrosslinked breath figure arrays.

    PubMed

    Ding, Lei; Zhang, Aijuan; Li, Wenqing; Bai, Hua; Li, Lei

    2016-01-01

    Multi-length scale porous polymer (MLSPP) films were fabricated using commercially available polystyrene (PS) via static breath figure (BF) process and sequent hypercrosslinking reaction. One level of ordered pores in microscale were introduced using static BF process, and the other level in nanoscale were produced by the sequent Friedel-Crafts hypercrosslinking reaction. The chemical structure of the PS MLSPP film was investigated by Fourier transformation infrared spectrometry and solid state nuclear magnetic resonance, and the morphology of the film was observed with electron microscopes. The MLSPP films showed large specific surface areas and excellent chemical and thermal stabilities, owing to the micropores and the crosslinked chemical structure produced by the Friedel-Crafts reaction. The methodology reported in this paper is a template-free, low cost and general strategy for the preparation of MLSPP films, which has potential applications in the areas of environment and energy. PMID:26397926

  1. Water Vapor Permeation of Metal Oxide/Polymer Coated Plastic Films

    NASA Astrophysics Data System (ADS)

    Numata, Yukihiro; Oya, Toshiyuki; Kuwahara, Mitsuru; Ito, Katsuya

    Barrier performance to water vapor permeation of ceramic coated layers deposited on flexible polymer films is of great interest to food packaging, medical device packaging and flat panel display industries. In this study, a new type film in which a ceramic layer is deposited on a polymer coated film was proposed for lower water vapor permeation. It is important how to control interfacial properties between each layer and film for good barrier performance. Several kinds of polymer coated materials were prepared for changing surface free energy of the films before and after depositing the ceramic layer. The ceramic layer, which is composed of mixed material of SiO2 and Al2O3, was adopted under the same conditions. The following results were obtained; 1) Water vapor permeation is not related to the surface energy of polymer coated films, 2) After depositing the ceramic layer, however, a strong correlation is observed between the water vapor permeation and surface free energy. 3) The phenomenon is considered that the polarity of the polymer layers plays a key role in changing the structure of ceramic coated layers.

  2. Tackling Mg alloy corrosion by natural polymer coatings-A review.

    PubMed

    Heise, Svenja; Virtanen, Sannakaisa; Boccaccini, Aldo R

    2016-10-01

    The field of protective coatings for magnesium and its alloys (e.g., AZ31) using natural polymers is reviewed. Polymers utilized are broadly divided into polysaccharides and proteins. For both polymer classes examples are given focusing on coating processing and characterization. Several analysing methods reported in literature are summarized highlighting the different characterization approaches applied in different studies, which makes difficult a direct comparison of the outcomes. In most cases, the protective behavior of coatings was determined using electrochemical impedance spectroscopy or by assessing hydrogen evolution in different fluids. Mechanical tests and in vitro cell culture studies have been also carried out on selected coating systems. Overall, the results show the possibility of applying protective coatings based on natural polymers on magnesium and its alloys, however, in vivo investigations are scarce so that long-term results in relevant conditions are not yet available. A comparison with the use of synthetic polymers is presented and current challenges and areas for future research are discussed, highlighting the need for further investigations in the field, which should enable broadening the applications of Mg and Mg alloys in medicine. © 2016 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 104A: 2628-2641, 2016. PMID:27159153

  3. Cementless porous-coated total knee arthroplasty: 10-year results in a consecutive series.

    PubMed

    Schrøder, H M; Berthelsen, A; Hassani, G; Hansen, E B; Solgaard, S

    2001-08-01

    We report the results of 114 AGC 2000 porous-coated, cementless total knee arthroplasties (TKA) performed consecutively in 102 patients during the period 1984-1986. After 10 years, 58 TKAs in 52 patients were evaluated with patient assessment, Hospital for Special Surgery knee score, weight-bearing radiographs done under fluoroscopic control, and survivorship analysis. All dropouts within the first 9 years were patients dying with a functioning TKA except 1 revision secondary to a supracondylar fracture after 8.5 years. Of the patients, 53 (92%) were satisfied or very satisfied with their TKA, and 55 (95%) of the knees were rated good or excellent. There was no pain in 53 knees, and the median knee flexion was 110 degrees. Six radiolucencies >1 mm were found beneath parts of the tibial component, and 5 radiolucencies were seen beneath the femoral component. None had progressed compared with the 5-year follow-up, and in all cases trabeculae could be seen reaching the prosthetic component. No migrations had occurred since the 5-year follow-up. No obvious joint space reduction was seen. Osteolysis presenting as an isolated cyst was found in 1 knee in the lateral tibial condyle and was not progressive. Two tibial components had been revised because of aseptic loosening and 1 because of septic loosening, all within the first 3 years. No femoral or patellar components were revised. The cumulative prosthesis survival rate after 10 to 11 years was 97%. When pain and radiographic loosening also were considered, the success rate was 87%. Cementless insertion of a nonmodular, porous-coated TKA resulted in a long-term durable bone-prosthesis interface. The flat-on-flat articulation did not result in catastrophic polyethylene wear or osteolysis within the first 10 years. PMID:11503114

  4. The efficient removal of endotoxins from insulin using quaternized polyethyleneimine-coated porous zirconia.

    PubMed

    McNeff, C; Zhao, Q; Almlöf, E; Flickinger, M; Carr, P W

    1999-10-15

    The synthesis and use of a zirconia-based, alkali-stable strong anion-exchange stationary phase are described for the removal of pyrogenic lipopolysaccharides (LPS) from insulin. The strong anion-exchange material is produced by deposition of polyethyleneimine (PEI) onto porous zirconia particles, followed by cross-linking with a novel reagent, 1,2-bis-(2-iodoethoxy) ethane, and quaternization with iodomethane. Physical characterization of the chromatographic support shows that it has an ion-exchange capacity of 0.6 mmol/g, and 82% of the amine sites on the surface are in quaternized form. Isocratic elution of small benzoic acid derivatives shows good column efficiency. The two primary virtues of this material are its chemical stability under alkali conditions (up to pH 13) and its lower hydrophobicity compared to previously described alkali-stable PEI-coated zirconia supports cross-linked with 1,10-diiododecane. Using this new zirconia-based phase, a purification protocol is developed for the efficient removal of Escherichia coli 0111:B4 LPS from bovine insulin samples. An endotoxin clearance rate of up to 1.3 x 10(8) was attained. Endotoxin levels were reduced to less than 5 endotoxin units/ml even at initial contamination levels as high as 5.0 x 10(6) endotoxin units/ml. Furthermore, endotoxin adsorbed to the porous zirconia column may be easily removed (depyrogenated) using alkali for repeated purification cycles. PMID:10527514

  5. Segment-Structured Diamond-Like Carbon Coatings on Polymer Catheter

    NASA Astrophysics Data System (ADS)

    Nakagawa, Taku; Ohishi, Ryusuke; Ohtake, Naoto; Takai, Osamu; Tsutsui, Nobumasa; Tsutsui, Yasuhiro; Muraki, Yasuhiro; Ogura, Jyunpei

    Diamond-like carbon (DLC) has remarkable mechanical and tribological properties. Besides those mechanical properties, it has been clarified that DLC shows high biocompatibility in recent years. DLC coating can give high strength, abrasion resistance, and biocompatibility for surface of substrates. Hence DLC is a candidate for the coating material for medical devices such as artificial organ, joint, catheter, etc. The objective of this study is to develop safety protection films for implantable medical polymer devices utilizing segment-structured DLC (S-DLC) coatings. S-DLC and continuous-structured DLC were deposited on polyurethane and nylon sheet for balloon catheters. As a result, friction coefficient of DLC coated polyurethane sheet was approximately one-sixth of that of pristine polyurethane sheet, and S-DLC showed very low friction coefficient of μ=0.1-0.15. DLC coating can prevent polyurethane sheet from worn out. The puncture-resistance of nylon sheets increased 0.2MPa on average by DLC coatings regardless of the film structure. It was confirmed that DLC inhibits adsorption of blood coagulation factor. In conclusion, we succeed to verify that these DLC films can improve tribological property, abrasion-resistance, puncture-resistance, and anti-thrombogenicity of polymer catheters. Moreover, segment-structured DLC films exhibits high performance for protection of polymer material for polymer catheters.

  6. Porous coordination polymers with ubiquitous and biocompatible metals and a neutral bridging ligand.

    PubMed

    Noro, Shin-ichiro; Mizutani, Junya; Hijikata, Yuh; Matsuda, Ryotaro; Sato, Hiroshi; Kitagawa, Susumu; Sugimoto, Kunihisa; Inubushi, Yasutaka; Kubo, Kazuya; Nakamura, Takayoshi

    2015-01-01

    The design of inexpensive and less toxic porous coordination polymers (PCPs) that show selective adsorption or high adsorption capacity is a critical issue in research on applicable porous materials. Although use of Group II magnesium(II) and calcium(II) ions as building blocks could provide cheaper materials and lead to enhanced biocompatibility, examples of magnesium(II) and calcium(II) PCPs are extremely limited compared with commonly used transition metal ones, because neutral bridging ligands have not been available for magnesium(II) and calcium(II) ions. Here we report a rationally designed neutral and charge-polarized bridging ligand as a new partner for magnesium(II) and calcium(II) ions. The three-dimensional magnesium(II) and calcium(II) PCPs synthesized using such a neutral ligand are stable and show selective adsorption and separation of carbon dioxide over methane at ambient temperature. This synthetic approach allows the structural diversification of Group II magnesium(II) and calcium(II) PCPs. PMID:25592677

  7. Porous coordination polymers with ubiquitous and biocompatible metals and a neutral bridging ligand

    PubMed Central

    Noro, Shin-ichiro; Mizutani, Junya; Hijikata, Yuh; Matsuda, Ryotaro; Sato, Hiroshi; Kitagawa, Susumu; Sugimoto, Kunihisa; Inubushi, Yasutaka; Kubo, Kazuya; Nakamura, Takayoshi

    2015-01-01

    The design of inexpensive and less toxic porous coordination polymers (PCPs) that show selective adsorption or high adsorption capacity is a critical issue in research on applicable porous materials. Although use of Group II magnesium(II) and calcium(II) ions as building blocks could provide cheaper materials and lead to enhanced biocompatibility, examples of magnesium(II) and calcium(II) PCPs are extremely limited compared with commonly used transition metal ones, because neutral bridging ligands have not been available for magnesium(II) and calcium(II) ions. Here we report a rationally designed neutral and charge-polarized bridging ligand as a new partner for magnesium(II) and calcium(II) ions. The three-dimensional magnesium(II) and calcium(II) PCPs synthesized using such a neutral ligand are stable and show selective adsorption and separation of carbon dioxide over methane at ambient temperature. This synthetic approach allows the structural diversification of Group II magnesium(II) and calcium(II) PCPs. PMID:25592677

  8. High-capacity magnetic hollow porous molecularly imprinted polymers for specific extraction of protocatechuic acid.

    PubMed

    Li, Hui; Hu, Xin; Zhang, Yuping; Shi, Shuyun; Jiang, Xinyu; Chen, Xiaoqin

    2015-07-24

    Magnetic hollow porous molecularly imprinted polymers (HPMIPs) with high binding capacity, fast mass transfer, and easy magnetic separation have been fabricated for the first time. In this method, HPMIPs was firstly synthesized using protocatechuic acid (PCA) as template, 4-vinylpyridine (4-VP) as functional monomer, glycidilmethacrylate (GMA) as co-monomer, and MCM-48 as sacrificial support. After that, epoxide ring of GMA was opened for chemisorbing Fe3O4 nanoparticles to prepare magnetic HPMIPs. The results of characterization indicated that magnetic HPMIPs exhibited large surface area (548m(2)/g) with hollow porous structure and magnetic sensitivity (magnetic saturation at 2.9emu/g). The following adsorption characteristics investigation exhibited surprisingly higher adsorption capacity (37.7mg/g), and faster kinetic binding (25min) than any previously reported PCA imprinted MIPs by traditional or surface imprinting technology. The equilibrium data fitted well to Langmuir equation and the adsorption process could be described by pseudo-second order model. The selective recognition experiments also demonstrated the high selectivity of magnetic HPMIPs towards PCA over analogues. The results of the real sample analysis confirmed the superiority of the proposed magnetic HPMIPs for selective and efficient enrichment of trace PCA from complex matrices. PMID:26044378

  9. Assessment of osteoinduction using a porous hydroxyapatite coating prepared by micro-arc oxidation on a new titanium alloy.

    PubMed

    Jing, Wensen; Zhang, Minghua; Jin, Lei; Zhao, Jian; Gao, Qing; Ren, Min; Fan, Qingyu

    2015-12-01

    Surface modification and material improvement is now an important way to improve the osseointegration between bone and uncemented prothesis. The purpose of this study was to investigate the bone ingrowth potential of porous hydroxyapatite (HA) coatings prepared by micro-arc oxidation (MAO) on Ti-3Zr-2Sn-3Mo-25Nb, a new titanium alloy. HA-coated specimens were implanted in the left proximal femoral medullary canal of beagles for 4, 12, and 24 weeks, and uncoated specimens were implanted in the right as a control. The surface morphology and phase composition were investigated with environmental scanning electron microscopy and X-ray diffractometry. The bone ingrowth was assessed by histomorphometry. A pull-out test was performed to assess the mechanical performance of the bone-implant interface. A porous coating was well prepared on the new titanium alloy by using the MAO method. The bone-to-implant contact was significantly higher for the HA-coated group compared to that in the uncoated group. Mechanical tests showed that the HA-coated group had significantly higher maximum force at the bone-implant interface compared to the uncoated specimens. MAO is a suitable coating approach for this new titanium alloy. The HA coating prepared by this approach can significantly promote bone ingrowth and the mechanical performance of the bone-implant interface. PMID:26306772

  10. Polymer-coated fibrous materials as the stationary phase in packed capillary gas chromatography.

    PubMed

    Saito, Yoshihiro; Tahara, Ai; Imaizumi, Motohiro; Takeichi, Tsutomu; Wada, Hiroo; Jinno, Kiyokatsu

    2003-10-15

    Synthetic polymer filaments have been introduced as the support material in packed capillary gas chromatography (GC). The filaments of the heat-resistant polymers, Zylon, Kevlar, Nomex, and Technora, were longitudinally packed into a short fused-silica capillary, followed by the conventional coating process for open-tubular GC columns. The separation of several test mixtures such as n-alkylbenzenes and n-alkanes was carried out with these polymer-coated fiber-packed capillary columns. With the coating by various polymeric materials on the surface of these filaments, the retentivity was significantly improved over the parent fiber-packed column (without polymer coating) as well as a conventional open-tubular capillary of the same length. The results demonstrated a good combination of Zylon as the support and poly(dimethylsiloxane)-based materials as the coating liquid-phase for the successful GC separation of n-alkanes and polycyclic aromatic hydrocarbons (PAHs), while successful applications for other separations such as poly(ethylene glycol) coating for the separation of alcohols were also obtained. From the results it has been suggested that the selectivity of the fiber-packed column could be tuned by selecting different coating materials, indicating the promising possibility for a novel usage of fine fibrous polymers as the support material that can be combined with newly synthesized coating materials specially designed for particular separations. Taking advantage of good thermal stability of the fibers, the column temperature could be elevated to higher than 350 degrees C with the combination of a short metallic capillary. PMID:14710834

  11. Accelerated cell-surface interlocking on plasma polymer-modified porous ceramics.

    PubMed

    Rebl, Henrike; Finke, Birgit; Schmidt, Jürgen; Mohamad, Heba S; Ihrke, Roland; Helm, Christiane A; Nebe, J Barbara

    2016-12-01

    Excellent osseointegration of permanent implants is crucial for the long lasting success of the implantation. To improve the osseointegrative potential, bio-inert titanium alloy surfaces (Ti6Al4V) are modified by plasma chemical oxidation (PCO®) of the titanium-oxide layer to a non-stoichiometric, amorphous calcium phosphate layer. The native titanium-oxide film measuring only a few nanometers is converted by PCO® to a thick porous calcium phosphate layer of about 10μm. In a second step the PCO surface is combined with a cell adhesive plasma-polymerized allylamine (PPAAm) nano film (5 and 50nm). Independent of the PPAAm coating homogeneity, the human osteoblast-like MG-63 cells show a remarkable increase in cell size and well-developed filopodia. Analyses of the actin cytoskeleton reveal that the cells mold to the pore shape of the PPAAm-covered PCO, thereby establishing a strong attachment to the surface. Interestingly, we could demonstrate that even though our untreated PCO shows excellent hydrophilicity, this alone is not sufficient to facilitate fast cell spreading, but the positive surface charges mediated by PPAAm. This multilayer composite material guarantees enhanced interlocking of the cells with the porous surface. PMID:27612809

  12. Effects of hydrophilic macropore fillings and coatings on the infiltration into water repellent porous media

    NASA Astrophysics Data System (ADS)

    Suetsugu, A.; Mori, Y.

    2012-12-01

    Macropores generate rapid flow paths in the surface soils by their high permeability under saturated/near-saturated moisture conditions. In natural soils, some macropores are filled/coated with various materials including decayed plant roots (Meek et al., 1989), exudates from plants/soil organisms (Jegou et al., 2001), iron oxides or other precipitates from preferentially-introduced solutes/colloids to the macropores (Rasmussen et al., 2001), or the surrounding soils with reduced bulk density (Ela et al., 1992). When we expect infiltration into water repellent soils through macropores or hydrophilic patches created from the macropore cementation processes, hydrophilicity of the macropore fillings/coatings should be understood. In the present study, we conducted an infiltration experiment with water repellent porous media and some macropore fillings/coatings, in order to clarify the roles of hydrophilic macropore fillings/coatings in infiltration. Ponding depth and flow distribution were monitored with a micro-focus X-ray computational tomography apparatus (SMX-90CT, Shimadzu Corp., Kyoto, Japan) at 90 kV and 110 μA. Dilute CsCl(aq) (density: 1.04 Mg m-3) was used as the contrast media to avoid density-driven alteration of the flows. Water repellency of the samples was evaluated by the water drop penetration time (WDPT, Van't Woudt, 1959). A glass beads (mean diameter: 0.46 mm, BZ-04, ASONE Corp., Osaka, Japan) was used as water repellent porous media. The glass beads sample was packed in 50-mL polypropylene centrifugation tubes at 1.55 Mg m-3 bulk density. A 2-mm hole was made at the bottom of each centrifugation tube for ventilation. The hole was covered with mesh cloth. Macroporous structure was made at the center of each tube from the surface. Each macroporous structure had 4-mm diameter and 30-mm length. Six types of macropores were prepared including 1) no macropore, 2) empty macropore, 3) an aluminum (Al) pipe (4-mm inner diameter, 5-mm outer diameter), 4) a

  13. Improving the quality of polymer-coated urea with recycled plastic, proper additives, and large tablets.

    PubMed

    Yang, Yue-Chao; Zhang, Min; Li, Yuncong; Fan, Xiao-Hui; Geng, Yu-Qing

    2012-11-14

    Polymer-coated urea (PCU) has great potential for increasing crop production and enhancing nitrogen (N) fertilizer use efficiency, benefiting the ecosystem. However, current PCUs are used only in a limited market, and the main obstacle to the wider use of PCUs is high cost compared to that of conventional N fertilizers. In this study, the low cost PCU and large tablet polymer-coated urea (LTPCU) were prepared by using recycling polystyrene foam and various sealants as the coating materials. The structural and chemical characteristics of the coating shells of the coated fertilizers were examined. The N release characteristics of coated fertilizers were determined in 25 °C water under laboratory conditions. The relationship between the N release longevity and the amount of coating material and the percentage of different sealants were evaluated. The results indicated that recycling polystyrene foam was the ideal coating material of the controlled release fertilizer. The polyurethane that was synthesized by the reaction of castor oil and isocyanate was better than the wax as the additive to delay the N release rate of coated urea. The coating material used for LTPCU was 70-80% less than those used for commercial PCUs under the same N release longevity. The cost of the recycling polystyrene foam used for coating one ton of pure N of the LTPCU was about one-seventh to one-eighth of the cost of the traditional polymer used for the commercial PCU. The experimental data showed that the LTPCU with good controlled-release capacities, being economical and eco-friendly, could be promising for wide use in agriculture and horticulture. PMID:23094596

  14. Stable dispersions of polymer-coated graphitic nanoplatelets

    NASA Technical Reports Server (NTRS)

    Stankovich, Sasha (Inventor); Nguyen, Sonbinh T. (Inventor); Ruoff, Rodney S. (Inventor)

    2011-01-01

    A method of making a dispersion of reduced graphite oxide nanoplatelets involves providing a dispersion of graphite oxide nanoplatelets and reducing the graphite oxide nanoplatelets in the dispersion in the presence of a reducing agent and a polymer. The reduced graphite oxide nanoplatelets are reduced to an extent to provide a higher C/O ratio than graphite oxide. A stable dispersion having polymer-treated reduced graphite oxide nanoplatelets dispersed in a dispersing medium, such as water or organic liquid is provided. The polymer-treated, reduced graphite oxide nanoplatelets can be distributed in a polymer matrix to provide a composite material.

  15. Understanding the role of dip-coating process parameters in the mechanical performance of polymer-coated bioglass robocast scaffolds.

    PubMed

    Motealleh, Azadeh; Eqtesadi, Siamak; Perera, Fidel Hugo; Pajares, Antonia; Guiberteau, Fernando; Miranda, Pedro

    2016-12-01

    The effect of different dip-coating variables-solvent, deposition temperature and polymer concentration-on the mechanical performance of polycaprolactone-coated 45S5 bioglass robocast scaffolds is systematically analyzed in this work. The reproducible geometry of the scaffolds produced by this additive manufacturing technique makes them an optimal model system and facilitates the analysis. The results suggest that the mechanical performance of the hybrid scaffolds is improved monotonically with polymer concentration, but this concentration cannot be increased indefinitely if the macroporosity interconnectivity, and thus the scaffold׳s capacity to promote tissue ingrowth, are to be preserved. An optimal concentration, and therefore viscosity (~1-4Pas in the present case), exists for any given set of process variables (scaffold geometry and material, polymer, solvent and process temperature) that yields coatings with optimal reinforcement and minimal reduction of scaffold functionality. Solvent and process temperature do not directly affect the strengthening provided by the polymeric coating. However they can determine the maximum concentration at the critical viscosity, and thereby the maximum achievable mechanical performance of the resulting hybrid scaffold. PMID:27522314

  16. Long-term Survival of Allograft Murine Islets Coated via Covalently Stabilized Polymers

    PubMed Central

    Rengifo, Hernán R.; Giraldo, Jaime A.; Labrada, Irayme; Stabler, Cherie L.

    2014-01-01

    Clinical islet transplantation (CIT) has emerged as a promising treatment option for type 1 diabetes mellitus (T1DM); however, the anti-rejection drug regimen necessary to mitigate allograft islet rejection is undesirable. The use of polymeric coatings to immunocamouflage the transplant from host immune attack has great potential. We have recently developed alginate and poly(ethylene glycol) (PEG)-based polymers, functionalized with azide and phosphine, respectively, which form spontaneous and chemoselective crosslinks via the bioorthogonal Staudinger ligation scheme. Herein, we explored the utility of these polymers to form immunoprotective, ultrathin coatings on murine primary pancreatic islets. Resulting coatings were nontoxic, with unimpaired glucose stimulated insulin secretion. Transplantation of coated BALB/c (H-2d) islets into streptozotozin-induced diabetic C57BL/6 (H-2b) resulted in prompt achievement of normoglycemia, at a rate comparable to controls. A significant subset of animals receiving coated islets (57%) exhibited long-term (> 100 d) function, with robust islets observed upon explantation. Control islets rejected after 15 d (+/− 9 d). Results illustrate the capacity of chemoselectively functionalized polymers to form coatings on islets, imparting no detrimental effect to the underlying cells, with resulting coatings exhibiting significant protective effects in an allograft murine model. PMID:24497465

  17. Porous biphasic calcium phosphate ceramics coated with nano-hydroxyapatite and seeded with mesenchymal stem cells for reconstruction of radius segmental defects in rabbits.

    PubMed

    Hu, Jianzhong; Yang, Zhiming; Zhou, Yongchun; Liu, Yong; Li, Kaiyang; Lu, Hongbin

    2015-11-01

    The osteoconduction of porous biphasic calcium phosphate (BCP) ceramics has been widely reported. In a previous study, we demonstrated that applying a nano-hydroxyapatite (nHA) coating enhances the osteoinductive potential of BCP ceramics, making these scaffolds more suitable for bone tissue engineering applications. The aim of the present study was to determine the effects of reconstructing radius defects in rabbits using nHA-coated BCP ceramics seeded with mesenchymal stem cells (MSCs) and to compare the bone regeneration induced by different scaffolds. Radius defects were created in 20 New Zealand rabbits, which were divided into four groups by treatment: porous BCP ceramics (Group A), nHA-coated porous BCP ceramics (Group B), porous BCP ceramics seeded with rabbit MSCs (Group C), and nHA-coated porous BCP ceramics seeded with rabbit MSCs (Group D). After in vitro incubation, the cell/scaffold complexes were implanted into the defects. Twelve weeks after implantation, the specimens were examined macroscopically and histologically. Both the nHA coating and seeding with MSCs enhanced the formation of new bone tissue in the BCP ceramics, though the osteoinductive potential of the scaffolds with MSCs was greater than that of the nHA-coated scaffolds. Notably, the combination of nHA coating and MSCs significantly improved the bone regeneration capability of the BCP ceramics. Thus, MSCs seeded into porous BCP ceramics coated with nHA may be an effective bone substitute to reconstruct bone defects in the clinic. PMID:26449447

  18. Synthesis of flake-like graphene from nickel-coated polyacrylonitrile polymer

    PubMed Central

    2014-01-01

    Graphene can be synthesized from polyacrylonitrile (PAN) polymer through pyrolysis. A metal catalyst such as nickel (Ni) is required for the conversion of the polymer to graphene. The metal catalysts can be placed either atop or underneath the polymer precursor. We observed that spatially non-uniform and disconnected graphene was fabricated when PAN film coated with a Ni layer was pyrolyzed, resulting in flake-like graphene. Formation of the flake-like graphene is attributed to the dewetting of the Ni layer coated on the PAN film. Dewetting phenomenon can be reduced by decreasing the pyrolysis temperature, and hence, more uniform graphene could be prepared. The effects of Ni coating thickness and the pyrolysis temperature on the fabricated graphene have been experimentally analyzed. PMID:25489278

  19. Facile fabrication of MIL-103(Eu) porous coordination polymer nanostructures and their sorption and sensing properties.

    PubMed

    Liu, Qing; Yang, Ji-Min; Guo, Fan; Jin, Li-Na; Sun, Wei-Yin

    2016-04-01

    Nano/microscale lanthanide porous coordination polymer MIL-103(Eu) [Eu(BTB)] (H3BTB = 4,4',4''-benzene-1,3,5-triyl-tribenzoic acid) crystals have been fabricated at room temperature by a facile, convenient and environmentally friendly method. The structures of the products were confirmed by powder X-ray diffraction, and the crystal morphologies, including microrods, nanorods and nanospheres, were characterized by scanning electron microscopy. It is found that the addition of sodium acetate and the concentration of the reactants have an important impact on the morphology and size of the MIL-103(Eu) crystals. Gas adsorption measurements reveal that the products show high specific surface areas among the rare earth based coordination polymers and the MIL-103(Eu) nanorods can selectively adsorb CO2 over N2 under ambient conditions. Furthermore, all the products exhibit red emission corresponding to the (5)D0→(7)F2 transition of the Eu(iii) ion, and MIL-103(Eu) nanorods display sensitive and selective sensing for Cu(ii) ions and acetone molecules in solution. PMID:26940895

  20. Formation of highly adherent nano-porous alumina on Ti-based substrates: a novel bone implant coating.

    PubMed

    Briggs, E P; Walpole, A R; Wilshaw, P R; Karlsson, M; Pålsgård, E

    2004-09-01

    Thin, nano-porous, highly adherent layers of anodised aluminium formed on the surface of titanium alloys are being developed as coatings for metallic surgical implants. The layers are formed by anodisation of a 1-5 microm thick layer of aluminium which has been deposited on substrate material by electron beam evaporation. The surface ceramic layer so produced is alumina with 6-8 wt % phosphate ions and contains approximately 5 x 10(8) cm(-2) pores with a approximately 160 nm average diameter, running perpendicular to the surface. Mechanical testing showed the coatings' shear and tensile strength to be at least 20 and 10 MPa, respectively. Initial cell/material studies show promising cellular response to the nano-porous alumina. A normal osteoblastic growth pattern with cell number increasing from day 1 to 21 was shown, with slightly higher proliferative activity on the nano-porous alumina compared to the Thermanox control. Scanning electron microscopy (SEM) examination of the cells on the porous alumina membrane showed normal osteoblast morphology. Flattened cells with filopodia attaching to the pores and good coverage were also observed. In addition, the pore structure produced in these ceramic coatings is expected to be suitable for loading with bioactive material to enhance further their biological properties. PMID:15448410

  1. Polymer coating of porcine decellularized and cross-linked aortic grafts.

    PubMed

    Heidenhain, Christoph; Weichert, Wilko; Schmidmaier, Gerhard; Wildemann, Britt; Hein, Moritz; Neuhaus, Peter; Heise, Michael

    2010-07-01

    This article investigates a method of modifying and optimizing the biocompatibility of decellularized vascular bioimplants when treated with a specialized, drug eluting coating. For this purpose, we carried out aortic transplantations using a porcine model. Decellularized, cross-linked aortic grafts were coated with poly(D,L-lactide) (PDLLA). To this coating, we added the anticoagulant drug lepirudin which, following transplantation, would be linearly eluted. These aortic grafts are easily manipulated in surgery. It was shown that, as a result of the lepirudin-eluting coating, the rate of thrombogenesis was reduced and the patency rate was significantly improved. However, lumen-stenosing pseudointima developed in all of the transplants and was not effected by PDLLA coating. Furthermore, no evidence of recellularisation was documented. This trial demonstrates that polymer coating of decellularized tissue is possible. Neointimal hyperplasia and the absence of cellular repopulation mark the negative consequences of this concept. PMID:20524202

  2. Application of Flame-Sprayed Coatings as Heating Elements for Polymer-Based Composite Structures

    NASA Astrophysics Data System (ADS)

    Lopera-Valle, Adrián; McDonald, André

    2015-10-01

    Flame-sprayed nickel-chromium-aluminum-yttrium (NiCrAlY) and nickel-chromium (NiCr) coatings were deposited on fiber-reinforced polymer composites for use as heating elements of structures that were exposed to cold environments. Electrical current was applied to the coatings to increase the surface temperature by way of Joule heating. The surface temperature profiles of the coatings were measured under free and forced convection conditions at different ambient temperatures, ranging from -25 to 23 °C. It was found that at ambient air temperatures below 0 °C, the surface temperature of the coating remained above 0 °C for both the forced and free convection conditions, and there was a nearly homogeneous temperature distribution over the coating surface. This suggests that flame-sprayed coatings could be used as heating elements to mitigate ice accretion on structures, without the presence of areas of localized high temperature.

  3. Effect of polymer coatings on fatigue strength of aluminum alloy 2024 box beams

    NASA Technical Reports Server (NTRS)

    Nordmark, G. E.; Kelsey, R. A.

    1972-01-01

    Previous investigators have shown that polymer coatings raise the fatigue strength of metals tested in air to about the same level as that of uncoated specimens tested in vacuum. The results are given of tests to determine if a polymer coating would improve the fatigue strength of built-up aluminum alloy members simulating aircraft construction. Aluminum alloy 2024-T4 riveted box beams were subjected to constant amplitude fatigue tests in air as well as in salt water fog. The coating did not improve the fatigue strength of beams tested in either environment. This is believed to result from the fact that most failures originated at rivet holes, which were isolated from both the coating and the environment.

  4. The Addition of Graphene to Polymer Coatings for Improved Weathering

    DOE PAGESBeta

    Nuraje, Nurxat; Khan, Shifath I.; Misak, Heath; Asmatulu, Ramazan

    2013-01-01

    Graphene nanoflakes in different weight percentages were added to polyurethane top coatings, and the coatings were evaluated relative to exposure to two different experimental conditions: one a QUV accelerated weathering cabinet, while the other a corrosion test carried out in a salt spray chamber. After the exposure tests, the surface morphology and chemical structure of the coatings were investigated via atomic force microscopy (AFM) and Fourier transform infrared (FTIR) imaging. Our results show that the addition of graphene does in fact improve the resistance of the coatings against ultraviolet (UV) degradation and corrosion. It is believed that this process willmore » improve the properties of the polyurethane top coating used in many industries against environmental factors.« less

  5. Zero-valent Iron Emplacement in Permeable Porous Media Using Polymer Additions

    SciTech Connect

    Oostrom, Mart; Wietsma, Thomas W.; Covert, Matthew A.; Vermeul, Vince R.

    2007-02-15

    At the Hanford Site in Washington, an extensive In Situ Redox Manipulation (ISRM) permeable reactive barrier was installed to prevent chromate from reaching the Columbia River. However, chromium has been detected in several wells, indicating a premature loss of the reductive capacity in the aquifer. One possible cause for premature chromate breakthrough is associated with the presence of high-permeability zones in the aquifer. The potential emplacement of zero-valent iron (Fe0) into high-permeability Hanford sediments to enhance the barrier’s reductive capacity using shear-thinning fluids containing polymers was investigated in three-dimensional wedge-shaped aquifer models. Porous media were packed in the wedge-shaped flow cell to create either a heterogeneous layered system with a high-permeability zone between two low-permeability zones or a high-permeability channel surrounded by low-permeability materials. The injection flow rate, polymer type, polymer concentration, and injected pore volumes were determined based on preliminary short- and long-column experiments. The flow cell experiments indicated that iron concentration enhancements of at least 0.6% (w/w) could be obtained using moderate flow rates and injection of 30 pore volumes. The aqueous pressure increased by a maximum of 25 KPa during infiltration, but a decrease in permeability was not observed. Under optimal conditions, the 0.6% amended Fe0 concentration would provide approximately 20 times the average reductive capacity that is provided by the dithionite-reduced Fe (II) in the ISRM barrier.

  6. Fabrication of Ruthenium Nanoparticles in Porous Organic Polymers: Towards Advanced Heterogeneous Catalytic Nanoreactors.

    PubMed

    Mondal, John; Kundu, Sudipta K; Hung Ng, Wilson Kwok; Singuru, Ramana; Borah, Parijat; Hirao, Hajime; Zhao, Yanli; Bhaumik, Asim

    2015-12-21

    A novel strategy has been adopted for the construction of a copolymer of benzene-benzylamine-1 (BBA-1), which is a porous organic polymer (POP) with a high BET surface area, through Friedel-Crafts alkylation of benzylamine and benzene by using formaldehyde dimethyl acetal as a cross-linker and anhydrous FeCl3 as a promoter. Ruthenium nanoparticles (Ru NPs) were successfully distributed in the interior cavities of polymers through NaBH4, ethylene glycol, and hydrothermal reduction routes, which delivered Ru-A, Ru-B, and Ru-C materials, respectively, and avoided aggregation of metal NPs. Homogeneous dispersion, the nanoconfinement effect of the polymer, and the oxidation state of Ru NPs were verified by employing TEM, energy-dispersive X-ray spectroscopy mapping, cross polarization magic-angle spinning (13)C NMR spectroscopy, and X-ray photoelectron spectroscopy analytical tools. These three new Ru-based POP materials exhibited excellent catalytic performance in the hydrogenation of nitroarenes at RT (with a reaction time of only ≈ 30 min), with high conversion, selectivity, stability, and recyclability for several catalytic cycles, compared with other traditional materials, such as Ru@C, Ru@SiO2, and Ru@TiO2, but no clear agglomeration or loss of catalytic activity was observed. The high catalytic performance of the ruthenium-based POP materials is due to the synergetic effect of nanoconfinement and electron donation offered by the 3D POP network. DFT calculations showed that hydrogenation of nitrobenzene over the Ru (0001) catalyst surface through a direct reaction pathway is more favorable than that through an indirect reaction pathway. PMID:26572500

  7. Polydopamine--a nature-inspired polymer coating for biomedical science

    NASA Astrophysics Data System (ADS)

    Lynge, Martin E.; van der Westen, Rebecca; Postma, Almar; Städler, Brigitte

    2011-12-01

    Polymer coatings are of central importance for many biomedical applications. In the past few years, poly(dopamine) (PDA) has attracted considerable interest for various types of biomedical applications. This feature article outlines the basic chemistry and material science regarding PDA and discusses its successful application from coatings for interfacing with cells, to drug delivery and biosensing. Although many questions remain open, the primary aim of this feature article is to illustrate the advent of PDA on its way to become a popular polymer for bioengineering purposes.

  8. Fluorescent polymer coatings with tuneable sensitive range for remote temperature sensing.

    PubMed

    Barja, Beatriz C; Chesta, Carlos A; Atvars, Teresa D Z; Aramendía, Pedro F

    2013-12-01

    Polymer films of poly(vinyl alcohol) containing the fluorescent dyes 4-aminophthalimide (AP) or 6-propionyl-2-dimethylamino-naphthalene (Prodan) are used as temperature-sensitive fluorescent coatings for remote temperature sensing. Temperature can be obtained by a two-wavelength ratiometric-based emission intensity measurement. The coatings are sensitive in a 100K temperature range that can be tuned by polymer-solute interactions. The usable range is 200-300 K for AP and 280-380 K for Prodan. PMID:23896292

  9. High-sensitivity DNA biosensor based on optical fiber taper interferometer coated with conjugated polymer tentacle.

    PubMed

    Huang, Yunyun; Tian, Zhuang; Sun, Li-Peng; Sun, Dandan; Li, Jie; Ran, Yang; Guan, Bai-Ou

    2015-10-19

    A sensitive bio-probe to in situ detect unlabeled single-stranded DNA targets based on optical microfiber taper interferometer coated by a high ordered pore arrays conjugated polymer has been presented. The polymer coating serves as tentacles to catch single-stranded DNA molecules by π-π conjugated interaction and varies the surface refractive index of the optical microfiber. The microfiber taper interferometer translates the refractive index information into wavelength shift of the interference fringe. The sensor exhibits DNA concentration sensitivity of 2.393 nm/log M and the lowest detection ability of 10(-10) M or even lower. PMID:26480357

  10. Fabricating Nanometer-Thick Simultaneously Oleophobic/Hydrophilic Polymer Coatings via a Photochemical Approach.

    PubMed

    Wang, Yongjin; Dugan, Michael; Urbaniak, Brian; Li, Lei

    2016-07-01

    The simultaneously oleophobic/hydrophilic coatings are highly desirable in antifogging, oil-water separation, and detergent-free cleaning. However, such coatings require special chemical structure, i.e., perfluorinated backbone and polar end-groups, and are too expensive for real-life application. Here, we have developed an UV-based photochemical approach to make nanometer-thick perfluoropolyethers without polar end-groups, which are not intrinsically simultaneously oleophobic/hydrophilic but cost-effective, become simultaneously oleophobic/hydrophilic. The contact angle, ellipsometry, and X-ray photoelectron spectroscopy (XPS) results indicated that the UV irradiation results in the covalent bonding between the polymer and the substrate, which renders more ordered packing of polymer chains and thus the appropriately small interchain distance. As a result, the small water molecules penetrate the polymer network while large oil molecules do not. As a result, the oil contact angle is larger than the water contact angle and the coating shows the simultaneous oleophobicity/hydrophilicity. Moreover, we also demonstrated that this nanometer-thick simultaneously oleophobic/hydrophilic coating has improved long-term antifogging performance and detergent-free cleaning capability and is mechanically robust. The photochemical approach established here potentially can be applied on many other polymers and greatly accelerate the development and application of simultaneously oleophobic/hydrophilic coatings. PMID:27249169

  11. Enhanced Physical Stability of Amorphous Drug Formulations via Dry Polymer Coating.

    PubMed

    Capece, Maxx; Davé, Rajesh

    2015-06-01

    Although amorphous solid drug formulations may be advantageous for enhancing the bioavailability of poorly soluble active pharmaceutical ingredients, they exhibit poor physical stability and undergo recrystallization. To address this limitation, this study investigates stability issues associated with amorphous solids through analysis of the crystallization behavior for acetaminophen (APAP), known as a fast crystallizer, using a modified form of the Avrami equation that kinetically models both surface and bulk crystallization. It is found that surface-enhanced crystallization, occurring faster at the free surface than in the bulk, is the major impediment to the stability of amorphous APAP. It is hypothesized that a novel use of a dry-polymer-coating process referred to as mechanical-dry-polymer-coating may be used to inhibit surface crystallization and enhance stability. The proposed process, which is examined, simultaneously mills and coats amorphous solids with polymer, while avoiding solvents or solutions, which may otherwise cause stability or crystallization issues during coating. It is shown that solid dispersions of APAP (64% loading) with a small particle size (28 μm) could be prepared and coated with the polymer, carnauba wax, in a vibratory ball mill. The resulting amorphous solid was found to have excellent stability as a result of inhibition of surface crystallization. PMID:25902736

  12. A Novel Plasma-Sprayed Durable Thermal Barrier Coating with a Well-Bonded YSZ Interlayer Between Porous YSZ and Bond Coat

    NASA Astrophysics Data System (ADS)

    Li, Chang-Jiu; Li, Yong; Yang, Guan-Jun; Li, Cheng-Xin

    2012-06-01

    Atmospheric plasma-sprayed YSZ (yttria-stabilized zirconia) thermal barrier coatings (TBCs) are widely used in industrial gas turbine engines to protect the superalloy blades from failure. The failure of TBCs in service occurs by the spalling of YSZ coating. Crack propagation leading to the failure of plasma-sprayed TBCs usually occurs within the YSZ coating near the YSZ/bond coat interface. In the present study, a novel durable TBC consisting of a YSZ interlayer of well-bonded lamellae between the bond coat and the conventional YSZ porous top coat was introduced. The YSZ interlayer was deposited at different coating surface temperatures, which resulted in the formation of YSZ with significantly improved interlamellar bonding. The result shows that the thermal cyclic lifetime of the novel TBCs with the 20-30-μm-thick YSZ interlayer increased by a factor of 4 compared with that of the conventional one. The improved thermal cyclic lifetime was attributed to the controlled transition of the cracking path from near the YSZ/bond coat interface to the YSZ top layer. The effect of the YSZ interlayer thickness on the lifetime of TBCs was also investigated.

  13. Surfactant induced aggregation behavior of Merocyanine-540 adsorbed on polymer coated positively charged gold nanoparticles

    NASA Astrophysics Data System (ADS)

    Das, K.; Uppal, A.; Saini, R. K.

    2016-01-01

    Surfactant induced aggregation behavior of Merocyanine 540 adsorbed on polymer (PDD) coated gold nanoparticles (AuNP) is reported. The absorption band of the dye shifts to higher energy in the presence of free polymer and polymer coated AuNP implying aggregation. Addition of a negatively charged surfactant (SDS) induces multiple bands in the extinction spectrum of the dye adsorbed on nanoparticle surface. The highest (460 nm) and lowest (564 nm) energy bands of the dye become prominent at 10 and >50 μM SDS concentrations respectively (dye: 10 μM; AuNP: 100-200 pM). Based on earlier results the high energy band is likely to originate from dye aggregates and the low energy band is likely to originate from dye monomers. This is attributed to the interplay between polymer-surfactant and polymer-dye interactions at the AuNP surface. The extinction spectra of dye adsorbed at AuNP surface remain unaffected in the presence of a positively charged (CTAB) or a neutral surfactant (Tx-100), at low surfactant concentrations. However at higher surfactant concentrations (>60 μM) dye aggregation takes place which is attributed to dye-surfactant interactions. The fluorescence intensity of the dye quenched significantly but its lifetime increased in the presence of polymer coated AuNP. This is attributed to aggregation and reduction in the photoisomerization rate of the dye adsorbed on AuNP surface.

  14. Characterization of moisture-protective polymer coatings using differential scanning calorimetry and dynamic vapor sorption.

    PubMed

    Bley, O; Siepmann, J; Bodmeier, R

    2009-02-01

    The aim of this study was to evaluate the moisture-protective ability of different polymeric coatings. Free films and film-coated tablets (with cores containing freeze-dried garlic powder) were prepared using aqueous solutions/dispersions of hydroxypropyl methylcellulose (HPMC), Opadry AMB [a poly(vinylalcohol)-based formulation] and Eudragit E PO [a poly(methacrylate-methylmethacrylate)]. The water content of the systems upon open storage at 75% relative humidity (RH) and 22 degrees C (room temperature) was followed gravimetrically. Furthermore, polymer powders, free films and coated tablets were analyzed by differential scanning calorimetry (DSC) and dynamic vapor sorption (DVS). The type of polymer strongly affected the resulting water uptake kinetics of the free films and coated tablets. DSC analysis revealed whether or not significant physical changes occurred in the coatings during storage, and whether the water vapor permeability was water concentration dependent. Using DVS analysis the critical glass transition RH of Opadry AMB powder and Opadry AMB-coated tablets at 25 degrees C could be determined: 44.0% and 72.9% RH. Storage below these threshold values significantly reduces water penetration. Thus, DVS and DSC measurements can provide valuable information on the nature of polymers used for moisture protection. PMID:18481311

  15. The pre-clinical assessment of rapamycin-eluting, durable polymer-free stent coating concepts.

    PubMed

    Steigerwald, Kristin; Merl, Sabine; Kastrati, Adnan; Wieczorek, Anna; Vorpahl, Marc; Mannhold, Raimund; Vogeser, Michael; Hausleiter, Jörg; Joner, Michael; Schömig, Albert; Wessely, Rainer

    2009-02-01

    All four currently FDA-approved drug-eluting stents (DESs) contain a durable polymeric coating which can negatively impact vascular healing processes and eventually lead to adverse cardiac events. Aim of this study was the pre-clinical assessment of two novel rapamycin-eluting stent (RES) coating technologies that abstain from use of a durable polymer. Two distinctive RES coating technologies were evaluated in vitro and in the porcine coronary artery stent model. The R-poly(S) stent platform elutes rapamycin from a biodegradable polymer that is top coated with the resin shellac to minimize the amount of polymer. The R-pro(S) stent platform allows dual drug release of rapamycin and probucol, blended by shellac. HPLC-based determination of pharmacokinetics indicated drug release for more than 28 days. At 30 days, neointimal formation was found to be significantly decreased for both DESs compared to bare-metal stents. Assessment of vascular healing revealed absence of increased inflammation in both DESs, which is commonly observed in DES with non-erodible polymeric coating. In conclusion, the pre-clinical assessment of RESs with resin-based or dual drug coating indicated an adequate efficacy profile as well as a beneficial effect for vascular healing processes. These results encourage the transfer of these technologies to clinical evaluation. PMID:18990438

  16. Effects of rotational symmetry breaking in polymer-coated nanopores

    SciTech Connect

    Osmanović, D.; Hoogenboom, B. W.; Ford, I. J.; Kerr-Winter, M.; Eccleston, R. C.

    2015-01-21

    The statistical theory of polymers tethered around the inner surface of a cylindrical channel has traditionally employed the assumption that the equilibrium density of the polymers is independent of the azimuthal coordinate. However, simulations have shown that this rotational symmetry can be broken when there are attractive interactions between the polymers. We investigate the phases that emerge in these circumstances, and we quantify the effect of the symmetry assumption on the phase behavior of the system. In the absence of this assumption, one can observe large differences in the equilibrium densities between the rotationally symmetric case and the non-rotationally symmetric case. A simple analytical model is developed that illustrates the driving thermodynamic forces responsible for this symmetry breaking. Our results have implications for the current understanding of the behavior of polymers in cylindrical nanopores.

  17. Superiority of Graphene over Polymer Coatings for Prevention of Microbially Induced Corrosion

    PubMed Central

    Krishnamurthy, Ajay; Gadhamshetty, Venkataramana; Mukherjee, Rahul; Natarajan, Bharath; Eksik, Osman; Ali Shojaee, S.; Lucca, Don A.; Ren, Wencai; Cheng, Hui-Ming; Koratkar, Nikhil

    2015-01-01

    Prevention of microbially induced corrosion (MIC) is of great significance in many environmental applications. Here, we report the use of an ultra-thin, graphene skin (Gr) as a superior anti-MIC coating over two commercial polymeric coatings, Parylene-C (PA) and Polyurethane (PU). We find that Nickel (Ni) dissolution in a corrosion cell with Gr-coated Ni is an order of magnitude lower than that of PA and PU coated electrodes. Electrochemical analysis reveals that the Gr coating offers ~10 and ~100 fold improvement in MIC resistance over PU and PA coatings respectively. This finding is remarkable considering that the Gr coating (1–2 nm) is ~25 and ~4000 times thinner than the PA (40–50 nm), and PU coatings (20–80 μm), respectively. Conventional polymer coatings are either non-conformal when deposited or degrade under the action of microbial processes, while the electro-chemically inert graphene coating is both resistant to microbial attack and is extremely conformal and defect-free. Finally, we provide a brief discussion regarding the effectiveness of as-grown vs. transferred graphene films for anti-MIC applications. While the as-grown graphene films are devoid of major defects, wet transfer of graphene is shown to introduce large scale defects that make it less suitable for the current application. PMID:26350049

  18. Superiority of Graphene over Polymer Coatings for Prevention of Microbially Induced Corrosion

    NASA Astrophysics Data System (ADS)

    Krishnamurthy, Ajay; Gadhamshetty, Venkataramana; Mukherjee, Rahul; Natarajan, Bharath; Eksik, Osman; Ali Shojaee, S.; Lucca, Don A.; Ren, Wencai; Cheng, Hui-Ming; Koratkar, Nikhil

    2015-09-01

    Prevention of microbially induced corrosion (MIC) is of great significance in many environmental applications. Here, we report the use of an ultra-thin, graphene skin (Gr) as a superior anti-MIC coating over two commercial polymeric coatings, Parylene-C (PA) and Polyurethane (PU). We find that Nickel (Ni) dissolution in a corrosion cell with Gr-coated Ni is an order of magnitude lower than that of PA and PU coated electrodes. Electrochemical analysis reveals that the Gr coating offers ~10 and ~100 fold improvement in MIC resistance over PU and PA coatings respectively. This finding is remarkable considering that the Gr coating (1-2 nm) is ~25 and ~4000 times thinner than the PA (40-50 nm), and PU coatings (20-80 μm), respectively. Conventional polymer coatings are either non-conformal when deposited or degrade under the action of microbial processes, while the electro-chemically inert graphene coating is both resistant to microbial attack and is extremely conformal and defect-free. Finally, we provide a brief discussion regarding the effectiveness of as-grown vs. transferred graphene films for anti-MIC applications. While the as-grown graphene films are devoid of major defects, wet transfer of graphene is shown to introduce large scale defects that make it less suitable for the current application.

  19. Superiority of Graphene over Polymer Coatings for Prevention of Microbially Induced Corrosion.

    PubMed

    Krishnamurthy, Ajay; Gadhamshetty, Venkataramana; Mukherjee, Rahul; Natarajan, Bharath; Eksik, Osman; Ali Shojaee, S; Lucca, Don A; Ren, Wencai; Cheng, Hui-Ming; Koratkar, Nikhil

    2015-01-01

    Prevention of microbially induced corrosion (MIC) is of great significance in many environmental applications. Here, we report the use of an ultra-thin, graphene skin (Gr) as a superior anti-MIC coating over two commercial polymeric coatings, Parylene-C (PA) and Polyurethane (PU). We find that Nickel (Ni) dissolution in a corrosion cell with Gr-coated Ni is an order of magnitude lower than that of PA and PU coated electrodes. Electrochemical analysis reveals that the Gr coating offers ~10 and ~100 fold improvement in MIC resistance over PU and PA coatings respectively. This finding is remarkable considering that the Gr coating (1-2 nm) is ~25 and ~4000 times thinner than the PA (40-50 nm), and PU coatings (20-80 μm), respectively. Conventional polymer coatings are either non-conformal when deposited or degrade under the action of microbial processes, while the electro-chemically inert graphene coating is both resistant to microbial attack and is extremely conformal and defect-free. Finally, we provide a brief discussion regarding the effectiveness of as-grown vs. transferred graphene films for anti-MIC applications. While the as-grown graphene films are devoid of major defects, wet transfer of graphene is shown to introduce large scale defects that make it less suitable for the current application. PMID:26350049

  20. Preparation and characterization of PTFE coating in new polymer quartz piezoelectric crystal sensor for testing liquor products

    NASA Astrophysics Data System (ADS)

    Gu, Yu; Li, Qiang

    2015-07-01

    A new method was developed based on the electron beam vacuum dispersion (EBVD) technology to prepare the PTFE polymer coating of the new polymer quartz piezoelectric crystal sensor for testing liquor products. The new method was applied in the new EBVD equipment which we designed. A real-time system monitoring the polymer coating’s thickness was designed for the new EBVD equipment according to the quartz crystal microbalance (QCM) principle, playing an important role in preparing stable and uniform PTFE polymer coatings of the same thickness. 30 pieces of PTFE polymer coatings on the surface of the quartz crystal basis were prepared with the PTFE polymer ultrafine powder (purity ≥ 99.99%) as the starting material. We obtained 30 pieces of new PTFE polymer sensors. By using scanning electron microscopy (SEM), the structure of the PTFE polymer coating’s column clusters was studied. One sample from the 30 pieces of new PTFE polymer sensors was analysed by SEM in four scales, i.e., 400×, 1000×, 10000×, and 25000×. It was shown that under the condition of high bias voltage and low bias current, uniformly PTFE polymer coating could be achieved, which indicates that the new EBVD equipment is suitable for mass production of stable and uniform polymer coating. Project supported by the National High Technology Research and Development Program of China (Grant No. 2013AA030901).

  1. Polymer protective coating for wet deep silicon etching processes

    NASA Astrophysics Data System (ADS)

    Spencer, Mary; Ruben, Kim; Li, Chenghong; Williams, Paul; Flaim, Tony D.

    2003-01-01

    A need exists for spin-applied polymeric coatings to protect electronic circuitry and other sensitive structures on MEMS devices during deep silicon wet etching processes involving corrosive mixtures of aqueous acids and bases. The challenge exists in developing protective coatings that do not decompose or dissolve in the harsh etchants and, more importantly, that maintain good adhesion to the substrate during the sometimes long etching processes. We have developed a multilayer coating system that is stable and adheres well to silicon nitride and other semiconductor materials and affords chemical protection for at least eight hours in hot potassium hydroxide etchant. The same coating system is also compatible with concentrated hydrofluoric acid etchants, which can diffuse rapidly through many polymeric materials to attack the device substrate.

  2. Materials: A compilation. [considering metallurgy, polymers, insulation, and coatings

    NASA Technical Reports Server (NTRS)

    1974-01-01

    Technical information is provided for the properties and fabrication of metals and alloys, as well as for polymeric materials, such as lubricants, coatings, and insulation. Available patent information is included in the compilation.

  3. Electrochemical Deposition of Nanostructured Conducting Polymer Coatings on Neural Prosthetic Devices

    NASA Astrophysics Data System (ADS)

    Yang, Junyan; Martin, David

    2003-03-01

    Micromachined neural prosthetic devices facilitate the functional stimulation of and recording from the central nervous system (CNS). These devices have been fabricated to consist of silicon shanks that have gold or iridium sites along their surface. Our goal is to improve the biocompatibility and long-term performance of the neural prosthetic probes when they are implanted chronically in the brain. In our most recent efforts we have established that electrochemical polymerization can be used to deposit fuzzy coatings of conducting polymers specifically on the electrode sites. For neural prosthetic devices that are intended for long term implantation, we need to develop surfaces that provide intimate contact and promote efficient signal transport at the interface of the microelectrode array and brain tissue. We have developed methods to rapidly and reliably fabricate nanostructured conducting polymer coatings on the electrode probes using templated and surfactant-mediated techniques. Conducting polymer nanomushrooms and nanohairs of polypyrrole (PPy) were electrochemically polymerized onto the functional sites of neural probes by using either nanoporous block copolymers thin films, "track-etched" polycarbonate films or anodic aluminium oxide membranes as templates. Nanofibers of conducting polymers have also been successfully obtained by polymerizations in the presence of surfactants. The influence of current density, monomer concentration, surfactant concentration, and deposition charge on the thickness and morphology of the nanostructured conducting polymer coatings has been studied by optical, scanned probe, scanning electron and transmission electron microscopy. As compared with the normal nodular morphology of polypyrrole, the nanostructured morphologies grown from the neural electrode result in fuzzy coatings with extremely high surface area. The electrical properties of the polymer coatings were studied by Impedance Spectroscopy (IS) and Cyclic Voltammetry

  4. Pigments, Paints, Polymer Coatings, Lacquers, and Printing Inks

    NASA Astrophysics Data System (ADS)

    Ryntz, Rose A.

    Change is constant in the coatings market. As mergers, acquisitions, and partnerships take shape, consolidation and globalization remain prominent. The 80/20 rule (20% of the firms accounting for 80% of business) takes effect as the need for regulatory and environmental compliance continues to plague the market. In 1975, the United States alone supported about 2000 coatings companies. Today, there are less than half that many.

  5. Fabrication of mullite-bonded porous SiC ceramics from multilayer-coated SiC particles through sol-gel and in-situ polymerization techniques

    NASA Astrophysics Data System (ADS)

    Ebrahimpour, Omid

    second part of the project. Alumina sol was synthesized by the hydrolysis of Aluminum isopropoxide using the Yoldas method. Alumina sol was homogenous and had a needle-like shape with a thickness of 2--3 nm. Crystalline changes during the heating process of alumina sol were studied using XRD. In addition, Fourier transform infrared (FTIR) spectroscopy was performed to identify the functional groups on the alumina sol surface as a function of temperature. In the third part of the project, the feasibility of the in-situ polymerization technique was investigated to fabricate porous SiC ceramics. In this part, the mixture of SiC and calcined alumina powders were coated by polyethylene via in-situ polymerizing referred to as the polymerization compounding process in a slurry phase. The polymerization was conducted under very moderate operational conditions using the Ziegler-Natta catalyst system. Differential scanning calorimetry (DSC) and TGA analysis and morphological studies (SEM and TEM) revealed the presence of a high density of polyethylene on the surface of SiC and alumina powders. The amount of polymer was controlled by the polymerization reaction time. Most parts of particles were coated by a thin layer of polyethylene and polymer. The porous SiC ceramics, which were fabricated by these treated particles showed higher mechanical and physical properties compared to the samples made without any treatment. The relative intensity of mullite was higher compared to the samples prepared by the traditional process. The effects of the sintering temperature, forming pressure and polymer content were also studied on the physical and mechanical properties of the final product. In the last phase of this research work, the focus of the investigation was to take advantage of both the sol-gel processing and in-situ polymerization method to develop a new process to manufacture mullite-bonded porous SiC ceramic with enhanced mechanical and physical properties. Therefore, first the Si

  6. Cationic polymers for DNA origami coating - examining their binding efficiency and tuning the enzymatic reaction rates.

    PubMed

    Kiviaho, Jenny K; Linko, Veikko; Ora, Ari; Tiainen, Tony; Järvihaavisto, Erika; Mikkilä, Joona; Tenhu, Heikki; Nonappa; Kostiainen, Mauri A

    2016-06-01

    DNA origamis are fully tailored, programmable, biocompatible and readily functionalizable nanostructures that provide an excellent foundation for the development of sophisticated drug-delivery systems. However, the DNA origami objects suffer from certain drawbacks such as low cell-transfection rates and low stability. A great deal of studies on polymer-based transfection agents, mainly focusing on polyplex formation and toxicity, exists. In this study, the electrostatic binding between a brick-like DNA origami and cationic block-copolymers was explored. The effect of the polymer structure on the binding was investigated and the toxicity of the polymer-origami complexes evaluated. The study shows that all of the analyzed polymers had a suitable binding efficiency irrespective of the block structure. It was also observed that the toxicity of polymer-origami complexes was insignificant at the biologically relevant concentration levels. Besides brick-like DNA origamis, tubular origami carriers equipped with enzymes were also coated with the polymers. By adjusting the amount of cationic polymers that cover the DNA structures, we showed that it is possible to control the enzyme kinetics of the complexes. This work gives a starting point for further development of biocompatible and effective polycation-based block copolymers that can be used in coating different DNA origami nanostructures for various bioapplications. PMID:27219684

  7. Filling and Transcription Behavior of Molten Polymer Coating on Microstructures in Melt-Transcription-Molding Process

    NASA Astrophysics Data System (ADS)

    Ito, Hiroshi; Satoh, Isao; Saito, Takushi; Yakemoto, Kazutoshi

    To clarify the fabrication mechanism of molten polymer coating on microstructures such as optical display parts and bio-tip in Melt-Transcription-Molding (MTM) process, the transcription experiments between a metal stamper engraved with microstructures and a molten polymer (PC: polycarbonate and COC: cyclo-olefin copolymer) were carried out under various molding conditions (mold temperature, polymer temperature, polymer pressure and coating speed) and transcript results were evaluated from the dimensional aspect. In this study the complete transcription of the microstructures was obtained at mold temperature of 170°C for COC and 175°C for PC, respectively. However, the rim height of the microstructure was increased and its center depth was decreased, when lower mold temperatures were applied. From these experimental results, it was suggested that the adhesion force between a molten polymer filled with the microstructure and the metal mold surface plays an important role in fixing the transcript shape of the microstructure against the elastic recovery force and/or shrinkage by cooling. Furthermore, a model to explain the filling and transcription behavior of molten polymers was proposed from viscoelastic properties of each polymer, and it was confirmed that predicted microstructure geometries deduced with the model are well fitted with the transcript results which were experimentally obtained under various mold temperatures.

  8. Performance improvement of an ionic polymer metal composite actuator by parylene thin film coating

    NASA Astrophysics Data System (ADS)

    Kim, Seong Jun; Lee, In Taek; Lee, Ho-Young; Hyup Kim, Yong

    2006-12-01

    IPMC (ionic polymer-metal composite) is a kind of ionic EAP (electroactive polymer) which is actuated by the movement of cations combined with water molecules in the polymer. The cations and water molecules move due to the applied voltage on the metal electrodes which are located on both sides of the polymer. However, water contained in the polymer gradually evaporates during the actuation and this reduces the performance of the IPMC actuator. To suppress the water evaporation from the IPMC, waterproof material such as parylene, silicone rubber and other polymers were coated on the surface of the IPMC. The displacement, the force and the lifetime of the actuator were observed by using a laser displacement measurement system and a load cell. The water impermeability of the polymer coating with respect to time was measured on a hot plate. Results showed that the parylene coating effectively suppressed the water loss from the IPMC and enlarged the lifetime of the actuator dramatically. However, it was found that parylene has poor adhesion properties to the metal electrode. To improve the adhesion, plasma treatments of argon (Ar), oxygen (O2) and trifluoromethane (CHF3) were performed on the electrode surface before parylene coating. We evaluated the surface morphology change of the electrode after plasma treatment by SEM (scanning electron microscopy) and AFM (atomic force microscopy). In addition, a tape adhesion test and a peel test were performed for quantitative analysis of adhesion strength between the metal electrode and parylene. It was found that the argon plasma treatment was the most effective to improve the adhesion strength between the metal electrode and parylene.

  9. PERFORMANCE OF A POLYMER SEALANT COATING IN AN ARCTIC MARINE ENVIRONMENT.

    SciTech Connect

    MOSKOWITZ,P.; COWGILL,M.; GRIFFITH,A.; CHERNAENKO,L.; DIASHEV,A.; NAZARIAN,A.

    2001-02-25

    The feasibility of using a polymer-based coating, Polibrid 705, to seal concrete and steel surfaces from permanent radioactive contamination in an Arctic marine environment has been successfully demonstrated using a combination of field and laboratory testing. A mobile, self-sufficient spraying device was developed to specifications provided by the Russian Northern Navy and deployed at the RTP Atomflot site, Murmansk, Russia. Demonstration coatings were applied to concrete surfaces exposed to conditions ranging from indoor pedestrian usage to heavy vehicle passage and container handling in a loading dock. A large steel container was also coated with the polymer, filled with solid radwaste, sealed, and left out of doors, exposed to the full annual Arctic weather cycle. The 12 months of field testing gave rise to little degradation of the sealant coating, except for a few chips and gouge marks on the loading bay surface that were readily repaired. Contamination resulting from radwaste handling was easily removed and the surface was not degraded by contact with the decontamination agents. The field tests were accompanied by a series of laboratory qualification tests carried out at a research laboratory in St. Petersburg. The laboratory tests examined a variety of properties, including bond strength between the coating and the substrate, thermal cycling resistance, wear resistance, flammability, and ease of decontamination. The Polibrid 705 coating met all the Russian Navy qualification requirements with the exception of flammability. In this last instance, it was decided to restrict application of the coating to land-based facilities.

  10. PERFORMANCE OF A POLYMER SEALANT COATING IN AN ARCTIC MARINE ENVIRONMENT

    SciTech Connect

    MOSKOWITZ,P.; COWGILL,M.; GRIFFITH,A.; CHERNAENKO,L.; DIASHEV,A.; NAZARIAN,A.

    2001-02-25

    The feasibility of using a polymer-based coating, Polibrid 705, to seal concrete and steel surfaces from permanent radioactive contamination in an Arctic marine environment has been successfully demonstrated using a combination of field and laboratory testing. A mobile, self-sufficient spraying device was developed to specifications provided by the Russian Northern Navy and deployed at the RTP Atomflot site, Murmansk, Russia. Demonstration coatings were applied to concrete surfaces exposed to conditions ranging from indoor pedestrian usage to heavy vehicle passage and container handling in a loading dock. A large steel container was also coated with the polymer, filled with solid radwaste, sealed, and left out of doors, exposed to the full annual Arctic weather cycle. The 12 months of field testing gave rise to little degradation of the sealant coating, except for a few chips and gouge marks on the loading bay surface that were readily repaired. Contamination resulting from radwaste handling was easily removed and the surface was not degraded by contact with the decontamination agents. The field tests were accompanied by a series of laboratory qualification tests carried out at a research laboratory in St. Petersburg. The laboratory tests examined a variety of properties, including bond strength between the coating and the substrate, thermal cycling resistance, wear resistance, flammability, and ease of decontamination. The Polibrid 705 coating met all the Russian Navy qualification requirements with the exception of flammability. In this last instance, it was decided to restrict application of the coating to land-based facilities.

  11. Structural changes of polymer-coated microgranules and excipients on tableting investigated by microtomography using synchrotron X-ray radiation.

    PubMed

    Kajihara, Ryusuke; Noguchi, Shuji; Iwao, Yasunori; Suzuki, Yoshio; Terada, Yasuko; Uesugi, Kentaro; Itai, Shigeru

    2015-03-15

    Multiple-unit tablets consisting of polymer-coated microgranules and excipients have a number of advantageous pharmaceutical properties. Polymer-coated microgranules are known to often lose their functionality because of damage to the polymer coating caused by tableting, and the mechanism of polymer coating damage as well as the structural changes of excipients upon tableting had been investigated but without in-situ visualization and quantitative analysis. To elucidate the mechanism of coating damage, the internal structures of multiple-unit tablets were investigated by X-ray computed microtomography using synchrotron X-rays. Cross sectional images of the tablets with sub-micron spatial resolution clearly revealed that void spaces remained around the compressed excipient particles in the tablets containing an excipient composed of cellulose and lactose (Cellactose(®) 80), whereas much smaller void spaces remained in the tablets containing an excipient made of sorbitol (Parteck(®) SI 150). The relationships between the void spaces and the physical properties of the tablets such as hardness and disintegration were investigated. Damage to the polymer coating in tablets was found mainly where polymer-coated microgranules were in direct contact with each other in both types of tablets, which could be attributed to the difference in hardness of excipient particles and the core of the polymer-coated microgranules. PMID:25660069

  12. A hierarchically porous anatase TiO2 coated-WO3 2D IO bilayer film and its photochromic properties.

    PubMed

    Li, Hua; Wu, Huazhong; Xiao, Jiajia; Su, Yanli; Robichaud, Jacques; Brüning, Ralf; Djaoued, Yahia

    2016-01-18

    A hierarchically porous anatase TiO2 coated-WO3 2D inverse opal (IO) bilayer film was fabricated on ITO glass using a layer by layer route with a hierarchically porous TiO2 top layer and an ordered super-macroporous WO3 2D IO bottom layer. This novel TiO2 coated-WO3 2D IO bilayer film was evaluated for photochromic applications. PMID:26576930

  13. A shape-recovery polymer coating for the corrosion protection of metallic surfaces.

    PubMed

    Lutz, Alexander; van den Berg, Otto; Van Damme, Jonas; Verheyen, Karen; Bauters, Erwin; De Graeve, Iris; Du Prez, Filip E; Terryn, Herman

    2015-01-14

    Self-healing polymer coatings are a type of smart material aimed for advanced corrosion protection of metals. This paper presents the synthesis and characterization of two new UV-cure self-healing coatings based on acrylated polycaprolactone polyurethanes. On a macroscopic scale, the cured films all show outstanding mechanical properties, combining relatively high Young's modulus of up to 270 MPa with a strain at break above 350%. After thermal activation the strained films recover up to 97% of their original length. Optical and electron microscopy reveals the self-healing properties of these coatings on hot dip galvanized steel with scratches and microindentations. The temperature-induced closing of such defects restores the corrosion protection and barrier properties of the coating as shown by electrochemical impedance spectroscopy and scanning vibrating electrode technique. Therefore, such coatings are a complementary option for encapsulation-based autonomous corrosion protection systems. PMID:25517028

  14. Next-generation resorbable polymer scaffolds with surface-precipitated calcium phosphate coatings

    PubMed Central

    Kim, Jinku; Magno, Maria Hanshella R.; Ortiz, Ophir; McBride, Sean; Darr, Aniq; Kohn, Joachim; Hollinger, Jeffrey O.

    2015-01-01

    Next-generation synthetic bone graft therapies will most likely be composed of resorbable polymers in combination with bioactive components. In this article, we continue our exploration of E1001(1k), a tyrosine-derived polycarbonate, as an orthopedic implant material. Specifically, we use E1001(1k), which is degradable, nontoxic, and osteoconductive, to fabricate porous bone regeneration scaffolds that were enhanced by two different types of calcium phosphate (CP) coatings: in one case, pure dicalcium phosphate dihydrate was precipitated on the scaffold surface and throughout its porous structure (E1001(1k) + CP). In the other case, bone matrix minerals (BMM) such as zinc, manganese and fluoride were co-precipitated within the dicalcium phosphate dihydrate coating (E1001(1k) + BMM). These scaffold compositions were compared against each other and against ChronOS (Synthes USA, West Chester, PA, USA), a clinically used bone graft substitute (BGS), which served as the positive control in our experimental design. This BGS is composed of poly(lactide co-ε-caprolactone) and beta-tricalcium phosphate. We used the established rabbit calvaria critical-sized defect model to determine bone regeneration within the defect for each of the three scaffold compositions. New bone formation was determined after 2, 4, 6, 8 and 12 weeks by micro-computerized tomography (μCT) and histology. The experimental tyrosine-derived polycarbonate, enhanced with dicalcium phosphate dihydrate, E1001(1k) + CP, supported significant bone formation within the defects and was superior to the same scaffold containing a mix of BMM, E1001(1k) + BMM. The comparison with the commercially available BGS was complicated by the large variability in bone formation observed for the laboratory preparations of E1001(1k) scaffolds. At all time points, there was a trend for E1001(1k) + CP to be superior to the commercial BGS. However, only at the 6-week time point did this trend reach statistical significance

  15. In situ generation of functionality in a reactive haloalkane-based ligand for the design of new porous coordination polymers.

    PubMed

    Kanoo, Prakash; Matsuda, Ryotaro; Sato, Hiroshi; Li, Liangchun; Jeon, Hyung Joon; Kitagawa, Susumu

    2013-10-01

    Herein, we report new porous coordination polymers (PCPs) via a facile synthetic approach called "in situ generation of functionality in the ligand". Upon a synthetic process of PCPs, a neutral (-CH2OH) or a cationic functionality (-CH2-[4,4'-bipyridine](+)) was generated on a isophthalate ligand from a reactive haloalkane (-CH2Br) moiety, affording two new PCPs. The PCPs have two-dimensional layered structures with large potential solvent-accessible voids for CO2 adsorption. PMID:24016100

  16. Tackiness of acrylic and cellulosic polymer films used in the coating of solid dosage forms.

    PubMed

    Wesseling, M; Kuppler, F; Bodmeier, R

    1999-01-01

    The objective was to determine the tackiness of acrylic and cellulosic polymer films in order to make predictions on the tackiness (agglomeration) of coated dosage forms during coating and curing. Force-displacement curves of the detachment process of two polymeric films were used as a measure of tackiness. Various polymers (cellulosic (Aquacoat and acrylics (Eudragit RS 30D, L 30D, NE 30D)), plasticizers (triacetin, triethyl citrate, tributyl citrate, acetyltributyl citrate) and anti-tacking agents (talc and glyceryl monostearate) were investigated. The order of tackiness for films prepared from the different aqueous polymer dispersions was in order of Eudragit NE 30D > RS 30D > RL 30D > Aquacoat. The tackiness increased with increasing plasticizer concentration due to the softening of the polymer. A correlation between the minimum film formation temperature and the tackiness was observed, however, no correlation between the tackiness and the lipophilicity of the plasticizer was seen. Talc and glyceryl monostearate (GMS) reduced the tackiness of the films significantly, with GMS being effective at much lower concentrations. Curing of Eudragit RS 30D-coated theophylline beads at temperatures higher than 40 degrees C in an irreversible agglomeration of the beads and damage of the coating upon separation of the beads. This resulted in a faster release than with uncured beads. Blending the beads with talc just prior to the curing step eliminated the agglomeration and therefore film damage, even at a curing temperature of 60 degrees C. PMID:10234529

  17. Emergence of polymer-coated corn and soybean influenced by tillage and sowing date

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Early establishment of crops is vital for maximizing production in the northern US Corn Belt. No tillage often delays soil warming, thus sowing too early may compromise seed viability due to prolonged exposure to cold soil. Coating seed with a temperature-activated polymer may circumvent the adverse...

  18. Coating of Polyaniline with an Insulating Polymer to Improve the Power Efficiency of Electrorheological Fluids

    NASA Astrophysics Data System (ADS)

    Akhavan, J.; Slack, K.; Wise, V.; Block, H.

    Currents drawn under high fields often present practical limitations to electrorheological (ER) fluids usefulness. For heavy-duty applications where large torques have to be transmitted, the power consumption of a ER fluid can be considerable, and for such uses a current density of ~100μAcm-2 is often taken as a practical upper limit. This investigation was conducted into designing a fluid which has little extraneous conductance and therefore would demand less current. Selected semi-conducting polymers provide effective substrates for ER fluids. Such polymers are soft insoluble powdery materials with densities similar to dispersing agents used in ER formulations. Polyaniline is a semi-conducting polymer and can be used as an effective ER substrate in its emeraldine base form. In order to provide an effective ER fluid which requires less current polyaniline was coated with an insulating polymer. The conditions for coating was established for lauryl and methyl methacrylate. Results from static yield measurements indicate that ER fluids containing coated polyaniline required less current than uncoated polyaniline i.e. 0.5μAcm-2. The generic type of coating was also found to be important.

  19. Macro- and micro-nutrient release characteristics of three polymer-coated fertilizers: Theory and measurements

    Technology Transfer Automated Retrieval System (TEKTRAN)

    In spite of several published studies we have an incomplete understanding of the ion release mechanisms and characteristics of primary polymer-coated fertilizer (PCF) technologies. Here we extend current conceptual models describing release mechanisms and describe the critical effects of substrate m...

  20. NASA Glenn/AADC-Rolls Royce Collaborated to Measure Erosion Resistance on Coated Polymer Matrix Composites

    NASA Technical Reports Server (NTRS)

    Miyoshi, Kazuhisa; Sutter, James K.; Mondry, Richard; Ma, Kong; Horan, Dick; Naik, Subhash; Cupp, Randall

    2003-01-01

    Polymer matrix composites (PMCs) are increasingly used in aerospace and automotive applications because of their light weight and high strength-to-weight ratio relative to metals. However, a major drawback of PMCs is poor abrasion resistance, which restricts their use, especially at high temperatures. Simply applying a hard coating on PMCs to improve abrasion and erosion resistance is not effective since coating durability is short lived (ref. 1). Generally, PMCs have higher coefficients of thermal expansion than metallic or ceramic coatings have, and coating adhesion suffers because of poor interfacial adhesion strength. One technique commonly used to improve coating adhesion or durability is the use of bond coats that are interleaved between a coating and a substrate with vastly different coefficients of thermal expansion. An example of this remedy is the use of bondcoats for ceramic thermal barrier coatings on metallic turbine components (ref. 2). Prior collaborative research between the NASA Glenn Research Center and the Allison Advanced Development Company (AADC) demonstrated that bond coats sandwiched between PMCs and high-quality plasma-sprayed, erosion-resistant coatings substantially improved the erosion resistance of PMCs (ref. 3). One unresolved problem in this earlier collaboration was that there was no easy, accurate way to measure the coating erosion wear scar. Coating wear was determined by both profilometry and optical microscopy. Both techniques are time consuming. Wear measurement by optical microscopy requires sample destruction and does not provide a comprehensive measure of the entire wear volume. An even more subtle, yet critical, problem is that these erosion coatings contain two or more materials with different densities. Therefore, simply measuring specimen mass loss before and after erosion will not provide an accurate gauge for coating and/or substrate volume loss. By using a noncontact technique called scanning optical interferometry

  1. Improvement of water barrier property of paperboard by coating application with biodegradable polymers.

    PubMed

    Han, Jaejoon; Salmieri, Stéphane; Le Tien, Canh; Lacroix, Monique

    2010-03-10

    Biopolymeric coatings were prepared and applied onto paperboard to improve its water barrier property. To prepare whey protein isolate (WPI)/cellulose-based films, WPI and glycerol were dissolved in water with glutaraldehyde (cross-linking agent) and cellulose xanthate. The solution was cast, dried, and insolubilized by entrapment of WPI in regenerated cellulose. Films were combined with beeswax (BW) into a bilayer coating system and then applied onto paperboard by heating compression. Another coating solution consisting of poly(vinyl butyral) (PVB)/zein was prepared by dissolving poly(vinyl alcohol) (PVA) and zein in 70% ethanol with glutaraldehyde and butyraldehyde (functionalization agent). The PVB/zein solution was applied onto paperboard after BW was sprayed. The structure of the PVB/zein-based coatings was analyzed by Fourier transform infrared spectroscopy (FTIR). The water vapor barrier property of coated paperboards was evaluated by water vapor transmission rate (WVTR) measurements. From the FTIR spectra, PVA functionalization after cross-linking and efficient acetalization into PVB were confirmed. WPI/cellulose and PVB/zein coating treatments improved the water barrier properties of paperboard by decreasing the WVTR by 77-78%. Although the BW coating was more efficient (decrease of WVTR by 89%), bilayer coatings composed of BW and polymer coatings had a stronger barrier effect with a decrease of WVTR to 92-95%, hence approaching commercial attributes required to ensure water vapor barrier in paperboard-based food containers (10 g/m(2).day). These results suggest that surface coating by biodegradable polymers may be utilized for the manufacture of paperboard containers in industrial applications. PMID:20155911

  2. Modular Fabrication of Polymer Brush Coated Magnetic Nanoparticles: Engineering the Interface for Targeted Cellular Imaging.

    PubMed

    Oz, Yavuz; Arslan, Mehmet; Gevrek, Tugce N; Sanyal, Rana; Sanyal, Amitav

    2016-08-01

    Development of efficient and rapid protocols for diversification of functional magnetic nanoparticles (MNPs) would enable identification of promising candidates using high-throughput protocols for applications such as diagnostics and cure through early detection and localized delivery. Polymer brush coated magnetic nanoparticles find use in many such applications. A protocol that allows modular diversification of a pool of parent polymer coated nanoparticles will lead to a library of functional materials with improved uniformity. In the present study, polymer brush coated parent magnetic nanoparticles obtained using reversible addition-fragmentation chain transfer (RAFT) polymerization are modified to obtain nanoparticles with different "clickable" groups. In this design, trithiocarbonate group terminated polymer brushes are "grafted from" MNPs using a catechol group bearing initiator. A postpolymerization radical exchange reaction allows installation of "clickable" functional groups like azides and maleimides on the chain ends of the polymers. Thus, modified MNPs can be functionalized using alkyne-containing and thiol-containing moieties like peptides and dyes using the alkyne-azide cycloaddition and the thiol-ene conjugation, respectively. Using the approach outlined here, a cell surface receptor targeting cyclic peptide and a fluorescent dye are attached onto nanoparticle surface. This multifunctional construct allows selective recognition of cancer cells that overexpress integrin receptors. Furthermore, the approach outlined here is not limited to the installation of azide and maleimide functional groups but can be expanded to a variety of "clickable" groups to allow nanoparticle modification using a broad range of chemical conjugations. PMID:27406320

  3. Review on recent and advanced applications of monoliths and related porous polymer gels in micro-fluidic devices.

    PubMed

    Vázquez, Mercedes; Paull, Brett

    2010-06-01

    This review critically summarises recent novel and advanced achievements in the application of monolithic materials and related porous polymer gels in micro-fluidic devices appearing within the literature over the period of the last 5 years (2005-2010). The range of monolithic materials has developed rapidly over the past decade, with a diverse and highly versatile class of materials now available, with each exhibiting distinct porosities, pore sizes, and a wide variety of surface functionalities. A major advantage of these materials is their ease of preparation in micro-fluidic channels by in situ polymerisation, leading to monolithic materials being increasingly utilised for a larger variety of purposes in micro-fluidic platforms. Applications of porous polymer monoliths, silica-based monoliths and related homogeneous porous polymer gels in the preparation of separation columns, ion-permeable membranes, preconcentrators, extractors, electrospray emitters, micro-valves, electrokinetic pumps, micro-reactors and micro-mixers in micro-fluidic devices are discussed herein. Procedures used in the preparation of monolithic materials in micro-channels, as well as some practical aspects of the micro-fluidic chip fabrication are addressed. Recent analytical/bioanalytical and catalytic applications of the final micro-fluidic devices incorporating monolithic materials are also reviewed. PMID:20493286

  4. Dry particle coating of polymer particles for tailor-made product properties

    SciTech Connect

    Blümel, C. Schmidt, J. Dielesen, A. Sachs, M. Winzer, B. Peukert, W. Wirth, K.-E.

    2014-05-15

    Disperse polymer powders with tailor-made particle properties are of increasing interest in industrial applications such as Selective Laser Beam Melting processes (SLM). This study focuses on dry particle coating processes to improve the conductivity of the insulating polymer powder in order to assemble conductive devices. Therefore PP particles were coated with Carbon Black nanoparticles in a dry particle coating process. This process was investigated in dependence of process time and mass fraction of Carbon Black. The conductivity of the functionalized powders was measured by impedance spectroscopy. It was found that there is a dependence of process time, respectively coating ratio and conductivity. The powder shows higher conductivities with increasing number of guest particles per host particle surface area, i.e. there is a correlation between surface functionalization density and conductivity. The assembled composite particles open new possibilities for processing distinct polymers such as PP in SLM process. The fundamentals of the dry particle coating process of PP host particles with Carbon Black guest particles as well as the influence on the electrical conductivity will be discussed.

  5. Dry particle coating of polymer particles for tailor-made product properties

    NASA Astrophysics Data System (ADS)

    Blümel, C.; Schmidt, J.; Dielesen, A.; Sachs, M.; Winzer, B.; Peukert, W.; Wirth, K.-E.

    2014-05-01

    Disperse polymer powders with tailor-made particle properties are of increasing interest in industrial applications such as Selective Laser Beam Melting processes (SLM). This study focuses on dry particle coating processes to improve the conductivity of the insulating polymer powder in order to assemble conductive devices. Therefore PP particles were coated with Carbon Black nanoparticles in a dry particle coating process. This process was investigated in dependence of process time and mass fraction of Carbon Black. The conductivity of the functionalized powders was measured by impedance spectroscopy. It was found that there is a dependence of process time, respectively coating ratio and conductivity. The powder shows higher conductivities with increasing number of guest particles per host particle surface area, i.e. there is a correlation between surface functionalization density and conductivity. The assembled composite particles open new possibilities for processing distinct polymers such as PP in SLM process. The fundamentals of the dry particle coating process of PP host particles with Carbon Black guest particles as well as the influence on the electrical conductivity will be discussed.

  6. Polymer Coated CaAl-Layered Double Hydroxide Nanomaterials for Potential Calcium Supplement

    PubMed Central

    Kim, Tae-Hyun; Lee, Jeong-A; Choi, Soo-Jin; Oh, Jae-Min

    2014-01-01

    We have successfully prepared layered double hydroxide (LDH) nanomaterials containing calcium and aluminum ions in the framework (CaAl-LDH). The surface of CaAl-LDH was coated with enteric polymer, Eudragit®L 100 in order to protect nanomaterials from fast dissolution under gastric condition of pH 1.2. The X-ray diffraction patterns, Fourier transform infrared spectroscopy, scanning electron and transmission electron microscopy revealed that the pristine LDH was well prepared having hydrocalumite structure, and that the polymer effectively coated the surface of LDH without disturbing structure. From thermal analysis, it was determined that only a small amount (less than 1%) of polymer was coated on the LDH surface. Metal dissolution from LDH nanomaterials was significantly reduced upon Eudragit®L 100 coating at pH 1.2, 6.8 and 7.4, which simulates gastric, enteric and plasma conditions, respectively, and the dissolution effect was the most suppressed at pH 1.2. The LDH nanomaterials did not exhibit any significant cytotoxicity up to 1000 μg/mL and intracellular calcium concentration significantly increased in LDH-treated human intestinal cells. Pharmacokinetic study demonstrated absorption efficiency of Eudragit®L 100 coated LDH following oral administration to rats. Moreover, the LDH nanomaterials did not cause acute toxic effect in vivo. All the results suggest the great potential of CaAl-LDH nanomaterials as a calcium supplement. PMID:25490138

  7. Bioactivity of degradable polymer sutures coated with bioactive glass.

    PubMed

    Bretcanu, Oana; Verné, Enrica; Borello, Luisa; Boccaccini, Aldo R

    2004-08-01

    Novel bioactive materials have been prepared by coating violet resorbable Vicryl sutures with a bioactive glass powder derived from a co-precipitation method. Two techniques have been chosen for the composite preparation: pressing the sutures in a bed of glass powder and slurry-dipping of sutures in liquid suspensions of bioactive glass powders. The uniformity and thickness of the coatings obtained by the two methods were compared. The bioactivity of the sutures with and without bioactive glass coating was tested by soaking in an inorganic acellular simulated body fluid (SBF). The composite sutures were characterised by XRD, SEM and FTIR analyses before and after soaking in SBF solution to assess the formation of hydroxyapatite on their surfaces, which is a qualitative measure of their bioactivity. The possible use of bioactive sutures to produce tissue engineering scaffolds and as reinforcement of resorbable calcium phosphates is discussed. PMID:15477741

  8. Stabilization of 2D assemblies of silver nanoparticles by spin-coating polymers

    NASA Astrophysics Data System (ADS)

    Hu, Longyu; Pfirman, Aubrie; Chumanov, George

    2015-12-01

    Silver nanoparticles self-assembled on poly(4-vinylpyridine) modified surfaces were spin-coated with poly(methyl methacrylate), poly(butyl methacrylate) and polystyrene from anisole and toluene solutions. The polymers filled the space between the particles thereby providing stabilization of the assemblies against particle aggregation when dried or chemically modified. The polymers did not coat the top surface of the nanoparticles offering the chemical accessibility to the metal surface. This was confirmed by converting the stabilized nanoparticles into silver sulfide and gold clusters. Etching the nanoparticles resulted in crater-like polymeric structures with the cavities extending down to the underlying substrate. Electrochemical reduction of silver inside the craters was performed. The approach can be extended to other nanoparticle assemblies and polymers.

  9. Assay of weathering effects on protective polymer coatings using positron annihilation spectroscopy

    SciTech Connect

    Hulett, L.D. Jr.; Wallace, S.; Xu, Jun; Nielsen, B.; Szeles, Cs.; Lynn, K.G.; Pfau, J.; Schaub, A.

    1995-02-01

    Polymer coatings, both with and without pigments, have been subjected to solar radiation and water spray weathering. The degrees of penetration of the weathering effects have been measured by injecting positrons of varying energy, i.e. to variable depths, into the films and observing the Doppler broadening of the annihilation radiation. The method is capable of detecting changes due to weathering effects at very early stages, long before visual examination reveals degradation. As little as one week of exposure caused measurable changes in the polymer structure, which were reflected in the Doppler broadening. Given further development, positron spectroscopy could possibly become a useful complement to the other methods of determining weatherabilities of protective polymer coatings.

  10. Influence of interface on the formation process of polymer coatings on metal

    NASA Astrophysics Data System (ADS)

    Maksimova, O. G.; Maksimov, A. V.; Moiseeva, A. I.

    2016-03-01

    The purpose of this work is in development of the model that allows to investigate the conformations of macromolecules near the interface “dielectric-metal” depending on the conditions of formation of the polymer coating. In the modified model of “sticky tape”, one part of macromolecule is anchored to the metal surface while the other can be elongated due to effective mean (molecular) field of dipolar type formed by free ends of other chains. The dynamic Monte-Carlo method for Langmuir’s model is used for calculation of adhesion force taking into account the interaction energy of monomers with the metal surface. It is shown that conformation of polymer chain is defined by temperature conditions of its formation. The obtained results are confirmed by the data of production tests on polymer coatings in JSC “Severstal”.

  11. Molecularly Imprinted Polymer Coated Quantum Dots for Multiplexed Cell Targeting and Imaging.

    PubMed

    Panagiotopoulou, Maria; Salinas, Yolanda; Beyazit, Selim; Kunath, Stephanie; Duma, Luminita; Prost, Elise; Mayes, Andrew G; Resmini, Marina; Tse Sum Bui, Bernadette; Haupt, Karsten

    2016-07-11

    Advanced tools for cell imaging are of great interest for the detection, localization, and quantification of molecular biomarkers of cancer or infection. We describe a novel photopolymerization method to coat quantum dots (QDs) with polymer shells, in particular, molecularly imprinted polymers (MIPs), by using the visible light emitted from QDs excited by UV light. Fluorescent core-shell particles specifically recognizing glucuronic acid (GlcA) or N-acetylneuraminic acid (NANA) were prepared. Simultaneous multiplexed labeling of human keratinocytes with green QDs conjugated with MIP-GlcA and red QDs conjugated with MIP-NANA was demonstrated by fluorescence imaging. The specificity of binding was verified with a non-imprinted control polymer and by enzymatic cleavage of the terminal GlcA and NANA moieties. The coating strategy is potentially a generic method for the functionalization of QDs to address a much wider range of biocompatibility and biorecognition issues. PMID:27238424

  12. Nanoporous Conducting Polymer-Based Coatings in Microextraction Techniques for Environmental and Biomedical Applications.

    PubMed

    Szultka-Mlynska, Malgorzata; Olszowy, Pawel; Buszewski, Bogusław

    2016-05-01

    Biologically active compounds constitute a wide group of chemicals, therefore it is a big challenge to create sorbents that are sensitive as well as selective. Development of nanoporous sorbents based on conducting polymers has expanded the boundaries of detection and quantification. Additionally, electrochemical synthesis used to deposit polymeric coatings directly on solid supports makes it possible to control physico-chemical properties of such sorbents. Besides the development of new polymeric nanoporous materials, the question of selectivity needs to be addressed. One possibility, successfully adapted to solid-phase microextraction, is molecular imprinting. Coatings created with this technology allow obtaining higher selectivity, with sensitivity at a constantly high level. The main aim of this review is to present comprehensively the concept of nanoporous sorbents based on conducting polymers, possible coating methods with their characteristics, and their various applications. This article focuses on applications in environmental and biomedical analyses. PMID:26322903

  13. Composite materials obtained by the ion-plasma sputtering of metal compound coatings on polymer films

    NASA Astrophysics Data System (ADS)

    Khlebnikov, Nikolai; Polyakov, Evgenii; Borisov, Sergei; Barashev, Nikolai; Biramov, Emir; Maltceva, Anastasia; Vereshchagin, Artem; Khartov, Stas; Voronin, Anton

    2016-01-01

    In this article, the principle and examples composite materials obtained by deposition of metal compound coatings on polymer film substrates by the ion-plasma sputtering method are presented. A synergistic effect is to obtain the materials with structural properties of the polymer substrate and the surface properties of the metal deposited coatings. The technology of sputtering of TiN coatings of various thicknesses on polyethylene terephthalate films is discussed. The obtained composites are characterized by X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy dispersive X-ray spectroscopy (EDX), atomic force microscopy (AFM), and scanning tunneling microscopy (STM) is shown. The examples of application of this method, such as receiving nanocomposite track membranes and flexible transparent electrodes, are considered.

  14. Preparation of Porous Chitosan-Siloxane Hybrids Coated with Hydroxyapatite Particles

    PubMed Central

    Shirosaki, Yuki; Okamoto, Kohei; Hayakawa, Satoshi; Osaka, Akiyoshi; Asano, Takuji

    2015-01-01

    This paper describes the apatite deposition of chitosan-silicate porous hybrids derived from chitosan and γ-glycidoxypropyltrimethoxysilane (GPTMS) in alkaline phosphate solution. The preparation of porous hybrids with needle-like apatite on their surfaces is described. Following apatite deposition the porous hybrids maintained high porosity. The enzymatic degradation rate was low even after 6 months and the porous hybrids were very flexible and cut easily using surgical scissors. PMID:26078948

  15. Rupture of Extensively Porous Coated Stems. - A Case Series of 2 Patients

    PubMed Central

    Gallart, X; Claret, G; Garcia, S; Fernández-Valencia, JA; Riba, J

    2014-01-01

    Introduction: Mechanical failure of femoral stems of revision hip arthroplasty has been rarely reported. In the current study, the cause of two stem fractures, which occurred in vivo, was analysed with use of clinical and radiological data, and the functional result after revision is presented. Case Report: Two patients, A 70-year-old male and a 73-year-old female, both of Mediterranean ethnic, and both patients underwent a revision total hip replacement to an uncemmented extensively porous coated stem. Both stems suffered an implant fatigue in vivo at three years and at two years follow-up respectively. Conclusion: Revision total hip arthroplasty is a procedure that will be performed more often the following years due to aging of population. Any orthopaedic surgeon performing hip surgery should be aware of the risk factors that can lead to total hip arthroplasty failure. In the analysed cases we can learn that the main factors related to this failure included the use of a small size stem (inferior to 14mm), an inadequate proximal osseous support because of trochanteric osteotomy, and a reduced preoperative bone stock. Although the use of cables has not been stated as a predisposing factor, we consider that they could also play a role in the development of this rare complication. PMID:27298979

  16. Highly porous silica-polyaniline nanocomposite as a novel solid-phase microextraction fiber coating.

    PubMed

    Gholivand, Mohammad B; Abolghasemi, Mir M; Fattahpour, Peyman

    2012-01-01

    A highly porous fiber-coated SBA-15/polyaniline material was prepared for solid-phase microextraction (SPME). The SBA-15/polyaniline nanocomposite was synthesized via chemical polymerization. The prepared SBA-15/polyaniline particles were analyzed by scanning electron microscopy analysis. The prepared nanomaterial was immobilized onto a stainless steel wire for fabrication of the SPME fiber. The fiber was evaluated for the extraction of some polycyclic aromatic hydrocarbons (PAHs) from aqueous sample solutions in combination with gas chromatography-mass spectrometry (GC-MS). In optimum conditions (extraction temperature 60°C, extraction time 40 min, ionic strength 20%, stirring rate: 500 rpm, desorption temperature 260°C, desorption time 2 min), the repeatability for one fiber (n=3), expressed as relative standard deviation (RSD%), was between 5.3 and 8.6% for the test compounds. For deionized water, spiked with selected PAHs, the detection limits for the studied compounds were between 2 and 20 pg/mL. PMID:22144100

  17. Efficient solar photocatalytic activity of TiO2 coated nano-porous silicon by atomic layer deposition

    NASA Astrophysics Data System (ADS)

    Sampath, Sridhar; Maydannik, Philipp; Ivanova, Tatiana; Shestakova, Marina; Homola, Tomáš; Bryukvin, Anton; Sillanpää, Mika; Nagumothu, Rameshbabu; Alagan, Viswanathan

    2016-09-01

    In the present study, TiO2 coated nano-porous silicon (TiO2/PS) was prepared by atomic layer deposition (ALD) whereas porous silicon was prepared by stain etching method for efficient solar photocatalytic activity. TiO2/PS was characterized by FESEM, AFM, XRD, XPS and DRS UV-vis spectrophotometer. Absorbance spectrum revealed that TiO2/PS absorbs complete solar light with wave length range of 300 nm-800 nm and most importantly, it absorbs stronger visible light than UV light. The reason for efficient solar light absorption of TiO2/PS is that nanostructured TiO2 layer absorbs UV light and nano-porous silicon layer absorbs visible light which is transparent to TiO2 layer. The amount of visible light absorption of TiO2/PS directly increases with increase of silicon etching time. The effect of silicon etching time of TiO2/PS on solar photocatalytic activity was investigated towards methylene blue dye degradation. Layer by layer solar absorption mechanism was used to explain the enhanced photocatalytic activity of TiO2/PS solar absorber. According to this, the photo-generated electrons of porous silicon will be effectively injected into TiO2 via hetero junction interface which leads to efficient charge separation even though porous silicon is not participating in any redox reactions in direct.

  18. Synthesis of porous molecularly imprinted polymers for selective adsorption of glutathione

    NASA Astrophysics Data System (ADS)

    Song, Renyuan; Hu, Xiaoling; Guan, Ping; Li, Ji; Qian, Liwei; Wang, Chaoli; Wang, Qiaoli

    2015-03-01

    An effective approach overcome the classical deficiencies of biomolecules molecularly imprinted polymers (MIPs), that is, low binding capacity and slow mass transfer rate, is proposed. With glutathione (GSH) as target molecule, porous imprinted layers were fabricated according to our newly developed method the introduction of a mixture of acetontrile and dimethylsulfoxide as porogen in surface-initiated polymerization systems. The resultant MIPs particles exhibited a large surface area could remarkably improve the imprinting effect in relation to a significantly increased imprinting factor and mass transfer rate, compared to the MIPs prepared by using aqueous solution as solvent. The batch static binding tests were carried out to evaluate the adsorption kinetics, adsorption isotherms and selective recognition of the MIPs particles. The binding behavior followed the pseudo-second order kinetic model, revealing that the process was chemically carried out. Two binding isotherm models were applied to analyze equilibrium data, obtaining the best description by Langmuir isotherm model. In addition, the selective of separation and extraction of GSH from a mixture of GSH and its structural analogs could be achieved on the MIPs solid-phase extraction cartridge, indicating that the possibility for the separation and enrichment of the template from complicated matrices.

  19. Immobilization of trypsin on porous glycidyl methacrylate beads: effects of polymer hydrophilization.

    PubMed

    Malmsten; Larsson

    2000-10-01

    The immobilization of trypsin at porous glycidyl methacrylate (GMA-GDMA) beads was investigated. In particular, the effects of surface modification of the beads through hydrophilic polymers on the amount protein immobilized and on the extent of retained activity after immobilization were adressed. Furthermore, immobilization at unmodified and hydrophilized beads from aqueous solution was compared to that from a water-in-oil microemulsion. It was found that the amount trypsin immobilized at the unmodified GMA-GDMA beads was significantly higher than that at hydrophilized GMA-GDMA beads. However, also the extent of specific activity loss after immobilization was larger for the unmodified than for the hydrophilized beads. Despite the latter, however, the total activity displayed by the hydrophilized beads was comparable to the unmodified beads at best. On the other hand, by peforming the immobilization from the microemulsion a high immobilization yield can be reached even for the hydrophilized beads, which also results in a higher degree of retained activity in the latter case than obtained for immobilization at the unmodified beads. Using this approach therefore resulted in the highest total activity of the trypsin-activated GMA-GDMA beads. PMID:10915949

  20. Highly porous polymer-derived wollastonite-hydroxycarbonate apatite ceramics for bone regeneration.

    PubMed

    Fiocco, L; Li, S; Bernardo, E; Stevens, M M; Jones, J R

    2016-04-01

    A novel strategy was employed to synthesize highly porous wollastonite-hydroxycarbonate apatite ceramic scaffolds for bone regeneration. A commercial liquid preceramic polymer filled with micro-CaCO3 powders was foamed at low temperature (at 350 °C), using the decomposition of a hydrazine additive, and then converted into ceramic by a treatment at 700 °C. Hydroxycarbonate apatite was later developed by a phosphatization treatment of ceramized foams, in a P-rich solution, while wollastonite was obtained by a second firing, at 900 °C. The effectiveness of the method was proven by x-ray diffraction analysis, showing the presence of the two expected crystalline phases. Porosity, interconnect size distribution and mechanical strength were in the range that is thought to be suitable for bone regeneration in non-load bearing sites (compressive strength ≈ 3 MPa, porosity ≈ 90%, modal interconnect diameter ≈ 130-160 μm). In addition, bioactivity and ion release rate were assessed in simulated body fluid (SBF). MC3T3 osteoblast precursor cells were able to colonize the material in vitro through the pore architecture and expressed osteogenic markers. PMID:27066770

  1. Highly Stable and Porous Cross-Linked Polymers for Efficient Photocatalysis

    SciTech Connect

    Xie, Zhigang; Wang, Cheng; deKrafft, Kathryn E.; Lin, Wenbin

    2011-02-23

    Porous cross-linked polymers (PCPs) with phosphorescent [Ru(bpy)₃]{sup 2+} and [Ir(ppy)₂(bpy)]{sup +} building blocks were obtained via octacarbonyldicobalt (Co₂(CO)₈)-catalyzed alkyne trimerization reactions. The resultant Ru- and Ir-PCPs exhibited high porosity with specific surface areas of 1348 and 1547 m²/g, respectively. They are thermally stable at up to 350 °C in air and do not dissolve or decompose in all solvents tested, including concentrated hydrochloric acid. The photoactive PCPs were shown to be highly effective, recyclable, and reusable heterogeneous photocatalysts for aza-Henry reactions, α-arylation of bromomalonate, and oxyamination of an aldehyde, with catalytic activities comparable to those of the homogeneous [Ru(bpy)₃]{sup 2+} and [Ir(ppy)₂(bpy)]{sup +} photocatalysts. This work highlights the potential of developing photoactive PCPs as highly stable, molecularly tunable, and recyclable and reusable heterogeneous photocatalysts for a variety of important organic transformations.

  2. Stabilization of montmorillonite clay in porous media by high-molecular-weight polymers

    SciTech Connect

    Zaitoun, A.; Berton, N. )

    1992-05-01

    In this paper a dynamic method is proposed for checking the stability of clay in porous media for different brine conditions and the stabilizing effect provided by several anionic and nonionic high-molecular-weight polymers. The method consists of injecting brine at decreasing salinity levels into clayey sandpacks until unstabilized permeability reduction is reached from the dislodging of clay particles that become trapped in pore restrictions. The last stable state before clay destablization is characterized by a critical salinity concentration (CSC). As expected, montmorillonite clay 5% dispersed in a sandpack is more stable in the presence of KCl than NaCl brines, giving CSC values of 5,000 and 27,500 ppm, respectively. Polyacrylamides are much better clay stabilizers than carboxymethyl cellulose (CMC) or xanthan gum (XG), lowering the CSC of KCl to 1,000 to 2,000 ppm and the CSC of NaCl to 6,000 to 7,000 ppm. A low-molecular-weight shear-degraded polyacrylamide is shown to keep good stabilizing power without inducing the high permeability reduction values obtained after adsorption of high-molecular-weight products. In addition to preventing clay migration, polyacrylamides are also shown to inhibit clay swelling.

  3. Viscoelastic polymer flows and elastic turbulence in three-dimensional porous structures.

    PubMed

    Mitchell, Jonathan; Lyons, Kyle; Howe, Andrew M; Clarke, Andrew

    2016-01-14

    Viscoelastic polymer solutions flowing through reservoir rocks have been found to improve oil displacement efficiency when the aqueous-phase shear-rate exceeds a critical value. A possible mechanism for this enhanced recovery is elastic turbulence that causes breakup and mobilization of trapped oil ganglia. Here, we apply nuclear magnetic resonance (NMR) pulsed field gradient (PFG) diffusion measurements in a novel way to detect increased motion of disconnected oil ganglia. The data are acquired directly from a three-dimensional (3D) opaque porous structure (sandstone) when viscoelastic fluctuations are expected to be present in the continuous phase. The measured increase in motion of trapped ganglia provides unequivocal evidence of fluctuations in the flowing phase in a fully complex 3D system. This work provides direct evidence of elastic turbulence in a realistic reservoir rock - a measurement that cannot be readily achieved by conventional laboratory methods. We support the NMR data with optical microscopy studies of fluctuating ganglia in simple two-dimensional (2D) microfluidic networks, with consistent apparent rheological behaviour of the aqueous phase, to provide conclusive evidence of elastic turbulence in the 3D structure and hence validate the proposed flow-fluctuation mechanism for enhanced oil recovery. PMID:26477403

  4. Preparation of porous polymer monoliths featuring enhanced surface coverage with gold nanoparticles

    PubMed Central

    Lv, Yongqin; Alejandro, Fernando Maya; Fréchet, Jean M. J.

    2012-01-01

    A new approach to the preparation of porous polymer monoliths with enhanced coverage of pore surface with gold nanoparticles has been developed. First, a generic poly(glycidyl methacrylate-co-ethylene dimethacrylate) monolith was reacted with cystamine followed by the cleavage of its disulfide bonds with tris(2-carboxylethyl)phosphine which liberated the desired thiol groups. Dispersions of gold nanoparticles with sizes varying from 5 to 40 nm were then pumped through the functionalized monoliths. The materials were then analyzed using both energy dispersive X-ray spectroscopy and thermogravimetric analysis. We found that the quantity of attached gold was dependent on the size of nanoparticles, with the maximum attachment of more than 60 wt% being achieved with 40 nm nanoparticles. Scanning electron micrographs of the cross sections of all the monoliths revealed the formation of a non-aggregated, homogenous monolayer of nanoparticles. The surface of the bound gold was functionalized with 1-octanethiol and 1-octadecanethiol, and these monolithic columns were used successfully for the separations of proteins in reversed phase mode. The best separations were obtained using monoliths modified with 15, 20, and 30 nm nanoparticles since these sizes produced the most dense coverage of pore surface with gold. PMID:22542442

  5. Ammonia capture in porous organic polymers densely functionalized with Brønsted acid groups.

    PubMed

    Van Humbeck, Jeffrey F; McDonald, Thomas M; Jing, Xiaofei; Wiers, Brian M; Zhu, Guangshan; Long, Jeffrey R

    2014-02-12

    The elimination of specific environmental and industrial contaminants, which are hazardous at only part per million to part per billion concentrations, poses a significant technological challenge. Adsorptive materials designed for such processes must be engendered with an exceptionally high enthalpy of adsorption for the analyte of interest. Rather than relying on a single strong interaction, the use of multiple chemical interactions is an emerging strategy for achieving this requisite physical parameter. Herein, we describe an efficient, catalytic synthesis of diamondoid porous organic polymers densely functionalized with carboxylic acids. Physical parameters such as pore size distribution, application of these materials to low-pressure ammonia adsorption, and comparison with analogous materials featuring functional groups of varying acidity are presented. In particular, BPP-5, which features a multiply interpenetrated structure dominated by <6 Å pores, is shown to exhibit an uptake of 17.7 mmol/g at 1 bar, the highest capacity yet demonstrated for a readily recyclable material. A complementary framework, BPP-7, features slightly larger pore sizes, and the resulting improvement in uptake kinetics allows for efficient adsorption at low pressure (3.15 mmol/g at 480 ppm). Overall, the data strongly suggest that the spatial arrangement of acidic sites allows for cooperative behavior, which leads to enhanced NH3 adsorption. PMID:24456083

  6. Porous coordination polymers of diverse topologies based on a twisted tetrapyridylbiaryl: application as nucleophilic catalysts for acetylation of phenols.

    PubMed

    Seth, Saona; Venugopalan, Paloth; Moorthy, Jarugu Narasimha

    2015-01-26

    Porous coordination polymers (CPs) with partially uncoordinated pyridyl rings based on rationally designed polypyridyl linkers are appealing from the point of view of their application as nucleophilic catalysts. A D2d -symmetric tetradentate organic linker L, that is, 2,2',6,6'-tetramethoxy-3,3',5,5'-tetrakis(4-pyridyl)biphenyl, was designed and synthesized for metal-assisted self-assembly aimed at porous CPs. Depending on the nature of the metal ion and the counter anion, the ligand L is found to function as a 3- or 4-connecting building block leading to porous CPs of diverse topologies. The reaction of L with Zn(NO3 )2 and Cd(NO3 )2 yields porous 2 D CPs of "fes" topology, in which the tetrapyridyl linker L serves as a 3-connecting unit with its free pyridyl rings well exposed into the pores. The functional utility of these porous CPs containing uncoordinated pyridyl rings is demonstrated by employing them as efficient heterogeneous nucleophilic catalysts for acetylation of a number of phenols with varying electronic properties and reactivities. PMID:25430673

  7. Development of Polymer-Coated Glass Slides as Optical Oligonucleotide Microarrays

    PubMed Central

    Pourjahed, Atefeh; Rabiee, Mohammad; Tahriri, Mohammadreza

    2013-01-01

    Background The microarray technology is in needed of cost-effective, low background noise and stable substrates for successful hybridization and analysis. Methods In this research, we developed a three-dimentional stable and mechanically reliable microarray substrates by coating of two polymeric layers on standard microscope glass slides. For fabrication of these substrates, a thin film of oxidized agarose was prepared on the Poly-L-Lysine (PLL) coated glass slides. Unmodified oligonucleotide probes were spotted and immobilized on these double layered thin films by adsorption on the porous structure of the agarose film. Some of the aldehyde groups of the activated agarose linked covalently to PLL amine groups; on the other side, they bound to amino groups of adsorbed tail of biomolecules. These linkages were fixed by UV irradiation at 254 nm using a CL-1000 UV. These prepared substrates were compared to only agarose-coated and PLL-coated slides Results Atomic Force Microscope (AFM) results demonstrated that agarose provided three-dimensional surface which had higher loading and bindig capacity for biomolecules than PLL-coated surface which had two-dimensional surface. The nano-indentation tests demonstrated the prepared double coating was more reliable and flexible for mechanical robotic spotting. In addition, the repeated indentation on different substrates showed uniformity of coatings. The stability of novel coating was sufficient for hybridization process. The signal-to-noise ratio in hybridization reactions performed on the agarose-PLL coated substrates increased two fold and four fold compared to agarose and PLL coated substrates, respectively. Conclusion Finally, the agarose-PLL microarrays had the highest signal (2920) and lowest background signal (205) in hybridization, suggesting that the prepared slides are suitable in analyzing wide concentration range of analytes. PMID:24285999

  8. Selective, ultrathin membrane skins prepared by deposition of novel polymer films on porous alumina supports

    NASA Astrophysics Data System (ADS)

    Balachandra, Anagi Manjula

    Membrane-based separations are attractive in industrial processes because of their low energy costs and simple operation. However, low permeabilities often make membrane processes uneconomical. Since flux is inversely proportional to membrane thickness, composite membranes consisting of ultrathin, selective skins on highly permeable supports are required to simultaneously achieve high throughput and high selectivity. However, the synthesis of defect-free skins with thicknesses less than 50 nm is difficult, and thus flux is often limited. Layer-by-layer deposition of oppositely charged polyelectrolytes on porous supports is an attractive method to synthesize ultrathin ion-separation membranes with high flux and high selectivity. The ion-transport selectivity of multilayer polyelectrolyte membranes (MPMs) is primarily due to Donnan exclusion; therefore increase in fixed charge density should yield high selectivity. However, control over charge density in MPMs is difficult because charges on polycations are electrostatically compensated by charges on polyanions, and the net charge in the bulk of these films is small. To overcome this problem, we introduced a templating method to create ion-exchange sites in the bulk of the membrane. This strategy involves alternating deposition of a Cu2+-poly(acrylic acid) complex and poly(allylamine hydrochloride) on a porous alumina support followed by removal of Cu2+ and deprotonation to yield free -COO- ion-exchange sites. Diffusion dialysis studies showed that the Cl-/SO42-. Selectivity of Cu2+-templated membranes is 4-fold higher than that of membranes prepared in the absence of Cu2+. Post-deposition cross-linking of these membranes by heat-induced amide bond formation further increased Cl-/SO42- selectivity to values as high as 600. Room-temperature, surface-initiated atom transfer radical polymerization (ATRP) provides another convenient method for formation of ultrathin polymer skins. This process involves attachment of

  9. Phase Separation of Silicon-Containing Polymer/Polystyrene Blends in Spin-Coated Films.

    PubMed

    Li, Yang; Hu, Kai; Han, Xiao; Yang, Qinyu; Xiong, Yifeng; Bai, Yuhang; Guo, Xu; Cui, Yushuang; Yuan, Changsheng; Ge, Haixiong; Chen, Yanfeng

    2016-04-19

    In this Article, two readily available polymers that contain silicon and have different surface tensions, polydimethylsiloxane (PDMS) and polyphenylsilsequioxane (PPSQ), were used to produce polymer blends with polystyrene (PS). Spin-coated thin films of the polymer blends were treated by O2 reactive-ion etching (RIE). The PS constituent was selectively removed by O2 RIE, whereas the silicon-containing phase remained because of the high etching resistance of silicon. This selective removal of PS substantially enhanced the contrast of the phase separation morphologies for better scanning electron microscope (SEM) and atomic force microscope (AFM) measurements. We investigated the effects of the silicon-containing constituents, polymer blend composition, concentration of the polymer blend solution, surface tension of the substrate, and the spin-coating speed on the ultimate morphologies of phase separation. The average domain size, ranging from 100 nm to 10 μm, was tuned through an interplay of these factors. In addition, the polymer blend film was formed on a pure organic layer, through which the aspect ratio of the phase separation morphologies was further amplified by a selective etching process. The formed nanostructures are compatible with existing nanofabrication techniques for pattern transfer onto substrates. PMID:27052643

  10. Plasma deposition of antimicrobial coating on organic polymer

    NASA Astrophysics Data System (ADS)

    Rżanek-Boroch, Zenobia; Dziadczyk, Paulina; Czajkowska, Danuta; Krawczyk, Krzysztof; Fabianowski, Wojciech

    2013-02-01

    Organic materials used for packing food products prevent the access of microorganisms or gases, like oxygen or water vapor. To prolong the stability of products, preservatives such as sulfur dioxide, sulfites, benzoates, nitrites and many other chemical compounds are used. To eliminate or limit the amount of preservatives added to food, so-called active packaging is sought for, which would limit the development of microorganisms. Such packaging can be achieved, among others, by plasma modification of a material to deposit on its surface substances inhibiting the growth of bacteria. In this work plasma modification was carried out in barrier discharge under atmospheric pressure. Sulfur dioxide or/and sodium oxide were used as the coating precursors. As a result of bacteriological studies it was found that sulfur containing coatings show a 16% inhibition of Salmonella bacteria growth and 8% inhibition of Staphylococcus aureus bacteria growth. Sodium containing coatings show worse (by 10%) inhibiting properties. Moreover, films with plasma deposited coatings show good sealing properties against water vapor. Contribution to the Topical Issue "13th International Symposium on High Pressure Low Temperature Plasma Chemistry (Hakone XIII)", Edited by Nicolas Gherardi, Henryca Danuta Stryczewska and Yvan Ségui.

  11. Polymer coating of copper oxide nanoparticles increases nanoparticles uptake and toxicity in the green alga Chlamydomonas reinhardtii.

    PubMed

    Perreault, François; Oukarroum, Abdallah; Melegari, Silvia Pedroso; Matias, William Gerson; Popovic, Radovan

    2012-06-01

    Copper oxide nanoparticles (CuO NPs) are frequently used in a polymer-coated form, to be included in paints or fabrics for antimicrobial properties. Their application in antifouling paints may lead to the contamination of aquatic ecosystems. However, the toxicological risk of NPs in the environment is hard to evaluate due to a lack of knowledge on the mechanisms of NP interaction with biological systems. In this study, we investigated the effect of polymer coating on CuO NP toxicity in the green alga Chlamydomonas reinhardtii by comparing bare and polymer-coated CuO NPs prepared from the same CuO nanopowder. Both CuO NP suspensions were toxic to C. reinhardtii after 6 h treatment to concentrations of 0.005-0.04 g L(-1). Bare and polymer-coated CuO NPs induced a decrease of Photosystem II activity and the formation of reactive oxygen species. Polymer-coated CuO NP was found to be more toxic than the uncoated CuO NP. The higher toxicity of CS-CuO NP was mainly associated with the increased capacity of polymer-coated CuO NP to penetrate the cell compared to bare CuO NPs. These results indicates that the high toxicity of polymer-coated CuO NPs in algal cells results of intracellular interactions between NPs and the cellular system. PMID:22445953

  12. A “green” strategy to construct non-covalent, stable and bioactive coatings on porous MOF nanoparticles

    PubMed Central

    Agostoni, V.; Horcajada, P.; Noiray, M.; Malanga, M.; Aykaç, A.; Jicsinszky, L.; Vargas-Berenguel, A.; Semiramoth, N.; Daoud-Mahammed, S.; Nicolas, V.; Martineau, C.; Taulelle, F.; Vigneron, J.; Etcheberry, A.; Serre, C.; Gref, R.

    2015-01-01

    Nanoparticles made of metal-organic frameworks (nanoMOFs) attract a growing interest in gas storage, separation, catalysis, sensing and more recently, biomedicine. Achieving stable, versatile coatings on highly porous nanoMOFs without altering their ability to adsorb molecules of interest represents today a major challenge. Here we bring the proof of concept that the outer surface of porous nanoMOFs can be specifically functionalized in a rapid, biofriendly and non-covalent manner, leading to stable and versatile coatings. Cyclodextrin molecules bearing strong iron complexing groups (phosphates) were firmly anchored to the nanoMOFs' surface, within only a few minutes, simply by incubation with aqueous nanoMOF suspensions. The coating procedure did not affect the nanoMOF porosity, crystallinity, adsorption and release abilities. The stable cyclodextrin-based coating was further functionalized with: i) targeting moieties to increase the nanoMOF interaction with specific receptors and ii) poly(ethylene glycol) chains to escape the immune system. These results pave the way towards the design of surface-engineered nanoMOFs of interest for applications in the field of targeted drug delivery, catalysis, separation and sensing. PMID:25603994

  13. A “green” strategy to construct non-covalent, stable and bioactive coatings on porous MOF nanoparticles

    NASA Astrophysics Data System (ADS)

    Agostoni, V.; Horcajada, P.; Noiray, M.; Malanga, M.; Aykaç, A.; Jicsinszky, L.; Vargas-Berenguel, A.; Semiramoth, N.; Daoud-Mahammed, S.; Nicolas, V.; Martineau, C.; Taulelle, F.; Vigneron, J.; Etcheberry, A.; Serre, C.; Gref, R.

    2015-01-01

    Nanoparticles made of metal-organic frameworks (nanoMOFs) attract a growing interest in gas storage, separation, catalysis, sensing and more recently, biomedicine. Achieving stable, versatile coatings on highly porous nanoMOFs without altering their ability to adsorb molecules of interest represents today a major challenge. Here we bring the proof of concept that the outer surface of porous nanoMOFs can be specifically functionalized in a rapid, biofriendly and non-covalent manner, leading to stable and versatile coatings. Cyclodextrin molecules bearing strong iron complexing groups (phosphates) were firmly anchored to the nanoMOFs' surface, within only a few minutes, simply by incubation with aqueous nanoMOF suspensions. The coating procedure did not affect the nanoMOF porosity, crystallinity, adsorption and release abilities. The stable cyclodextrin-based coating was further functionalized with: i) targeting moieties to increase the nanoMOF interaction with specific receptors and ii) poly(ethylene glycol) chains to escape the immune system. These results pave the way towards the design of surface-engineered nanoMOFs of interest for applications in the field of targeted drug delivery, catalysis, separation and sensing.

  14. Micro-nanoprobing measurement of polymer coating/film mechanical properties

    NASA Astrophysics Data System (ADS)

    Xia, Xinyun (Sherry)

    2000-10-01

    The goals of this study are (1) to demonstrate the applications of nanoindentation for mechanical properties studies of polymer coating/film systems; (2) to develop and verify viscoelastic analytical solutions for indentation on polymers; (3) to advance nanoindentation technique for better understanding of coating processes, particularly under drying conditions. To meet the project goals, several polymer coating/film systems are studied during or after drying and curing. First, the demonstration experiments were mainly conducted on near-surface structure formation of chemically imidized polyimide films. Nanoindentation method successfully explained the peel strength difference observed in industry by distinguishing variation of microstructure related modulus difference between two sides of films with different annealing temperature. Second, to verify a linear viscoelastic analytical solutions based on standard solids model developed by Cheng et al, indentation creep and relaxation tests with flat-ended punch and spherical indenter were conducted on polystyrene, photographic protecting coatings and polyvinyl alcohol coatings (PVOH). The coatings' young's modulus and viscosity obtained were similar to literature values. The application of these solutions to PVOH coatings also successfully helped to distinguish the near surface crystallinity difference formed during the drying process. Furthermore, humidity and temperature control accessories are set up for Hysitron to extend the capability of nanoindentation method on in situ coating mechanical properties study. Influence on mechanical properties of drying semicrystalline PVOH coating with different molecular weight under different humidity was studied. The work first relates the near-surface mechanical property to solvent induced surface crystallinity during process and indicates that such approaches will help to optimize drying processes and coating microstructure control. To demonstrate the application of the

  15. Porous polymers bearing functional quaternary ammonium salts as efficient solid catalysts for the fixation of CO2 into cyclic carbonates.

    PubMed

    Cai, Sheng; Zhu, Dongliang; Zou, Yan; Zhao, Jing

    2016-12-01

    A series of porous polymers bearing functional quaternary ammonium salts were solvothermally synthesized through the free radical copolymerization of divinylbenzene (DVB) and functionalized quaternary ammonium salts. The obtained polymers feature highly cross-linked matrices, large surface areas, and abundant halogen anions. These polymers were evaluated as heterogeneous catalysts for the synthesis of cyclic carbonates from epoxides and CO2 in the absence of co-catalysts and solvents. The results revealed that the synergistic effect between the functional hydroxyl groups and the halide anion Br(-) afforded excellent catalytic activity to cyclic carbonates. In addition, the catalyst can be easily recovered and reused for at least five cycles without significant loss in activity. PMID:27365001

  16. PEDOT polymer coatings facilitate smaller neural recording electrodes

    PubMed Central

    Ludwig, Kip A.; Langhals, Nicholas B.; Joseph, Mike D.; Richardson-Burns, Sarah M.; Hendricks, Jeffrey L.; Kipke, Daryl R.

    2012-01-01

    We investigated using poly(3,4-ethylenedioxythiophene) (PEDOT) to lower the impedance of small, gold recording electrodes with initial impedances outside of the effective recording range. Smaller electrode sites enable more densely packed arrays, increasing the number of input and output channels to and from the brain. Moreover, smaller electrode sizes promote smaller probe designs; decreasing the dimensions of the implanted probe has been demonstrated to decrease the inherent immune response, a known contributor to the failure of long-term implants. As expected, chronically implanted control electrodes were unable to record well-isolated unit activity, primarily as a result of a dramatically increased noise floor. Conversely, electrodes coated with PEDOT consistently recorded high-quality neural activity, and exhibited a much lower noise floor than controls. These results demonstrate that PEDOT coatings enable electrode designs 15 microns in diameter. PMID:21245527

  17. Evaluation of the film-coating properties of a hydroxyethyl cellulose/hydroxypropyl methylcellulose polymer system.

    PubMed

    Li, Shun Por; Martellucci, Stephen A; Bruce, Richard D; Kinyon, Adam C; Hay, Michael B; Higgins, John D

    2002-04-01

    The effect of different grades of hydroxyethyl cellulose (HEC) and hydroxypropyl methllcellulose (HPMC) on the film-formation and taste-masking ability for ibuprofen granules was evaluated. Three batches of coated ibuprofen granules were prepared using a roto-granulator, each with a different coating composition. Two grades of HEC [MW300,000 (H) and MW90,000 (L)] were combined with three different grades of HPMC [MW 11,000 (L), MW 25,000 (M) and MW 35,000 (H)] to prepare the coating solutions. Mechanical strength and physical properties of the polymer films were evaluated. Films made from HPMC (L)/HEC (H), HPMC (M)/HEC (H), and HPMC (H)/HEC (H) were stronger and more flexible than the HPMC (L) HEC (L) films. The assay, dissolution, particle size distribution, and environmental scanning electron microscopy (ESEM) data of the three batches of the coated ibuprofen granules were similar. PMID:12056532

  18. High-temperature separation with polymer-coated fiber in packed capillary gas chromatography.

    PubMed

    Saito, Yoshihiro; Ogawa, Mitsuhiro; Imaizumi, Motohiro; Ban, Kazuhiro; Abe, Akira; Takeichi, Tsutomu; Wada, Hiroo; Jinno, Kiyokatsu

    2005-06-01

    High-temperature gas chromatographic separation of several synthetic polymer mixtures with Dexsil-coated fiber-packed columns was studied. A bundle of heat-resistant filaments, Zylon, was longitudinally packed into a short metal capillary, followed by the conventional coating process with Dexsil 300 material. Prior to the packing process the metal capillary was deactivated by the formation of a silica layer. The typical size of the resulting column was 0.3-mm i.d., 0.5-mm o.d., 1-m length, and packed with about 170 filaments of the Dexsil-coated Zylon. The column temperature could be elevated up to 450 degrees C owing to the good thermal stability of the fiber, Dexsil coating, and metal capillary; furthermore, this allowed the separation of low-volatile compounds to be studied. PMID:15933854

  19. Trypsin coatings on electrospun and alcohol-dispersed polymer nanofibers for trypsin digestion column

    SciTech Connect

    Jun, Seung-Hyun; Chang, Mun Seock; Kim, Byoung Chan; An, Hyo Jin; Lopez-Ferrer, Daniel; Zhao, Rui; Smith, Richard D.; Lee, Sang-Won; Kim, Jungbae

    2010-09-15

    The construction of a trypsin reactor in a chromatography column for rapid and efficient protein digestion in proteomics is described. Electrospun and alcohol-dispersed polymer nanofibers were used for the fabrication of highly stable trypsin coating, which was prepared by a two-step process of covalent attachment and enzyme crosslinking. In a comparative study with the trypsin coatings on asspun and non-dispersed nanofibers, it has been observed that a simple step of alcohol dispersion improved not only the enzyme loading but also the performance of protein digestion. In-column digestion of enolase was successfully performed in less than twenty minutes. By applying the alcohol dispersion of polymer nanofibers, the bypass of samples was reduced by filling up the column with well-dispersed nanofibers, and subsequently, interactions between the protein and the enzymes were improved yielding more complete and reproducible digestions. Regardless of alcohol-dispersion or not, trypsin coating showed better digestion performance and improved performance stability under recycled uses than covalently-attached trypsin. The combination of highly stable trypsin coating and alcoholdispersion of polymer nanofibers has opened up a new potential to develop a trypsin column for on-line and automated protein digestion.

  20. Reduced bleaching in organic nanofibers by bilayer polymer/oxide coating

    SciTech Connect

    Tavares, L.; Kjelstrup-Hansen, J.; Rubahn, H.-G.; Sturm, H.

    2010-05-15

    Para-hexaphenylene (p-6P) molecules exhibit a characteristic photoinduced reaction (bleaching) resulting in a decrease in luminescence intensity upon UV light exposure, which could render the technological use of the nanofibers problematic. In order to investigate the photoinduced reaction in nanofibers, optical bleaching experiments have been performed by irradiating both pristine and coated nanofibers with UV light. Oxide coating materials (SiO{sub x} and Al{sub 2}O{sub 3}) were applied onto p-6P nanofibers. These treatments caused a reduction in the bleaching reaction but in addition, the nanofiber luminescence spectrum was significantly altered. It was observed that some polymer coatings [a statistical copolymer of tetrafluoroethylene and 2,2-bis-trifluoromethyl-4,5-difluoro-1,3-dioxole, P(TFE-PDD), and poly(methyl methacrylate), PMMA] do not interfere with the luminescence spectrum from the p-6P but are not effective in stopping the bleaching. Bilayer coatings with first a polymer material, which should work as a protection layer to avoid modifications of the p-6P luminescence spectrum, and second an oxide layer used as oxygen blocker were tested and it was found that a particular bilayer polymer/oxide combination results in a significant reduction in bleaching without affecting significantly the emission spectrum from the nanofibers.