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Query: UMLS:C0432222 (SEM)
47,337 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Ultrathin TiO2 films showing rich morphologies are prepared on Si(100) substrates using sol-gel chemistry coupled with an amphilic polystyrene-block-poly(ethylene oxide) (PS-b-PEO) diblock copolymer as a structure-directing agent. The block copolymer undergoes a good-poor solvent pair induced phase separation in a mixed solution of 1,4-dioxane, concentrated hydrochloric acid (HCl), and titanium tetraisopropoxide (TTIP). By adjusting the weight fractions of 1,4-dioxane, HCl, and TTIP, inorganic block copolymer composite films containing a variety of different morphologies are obtained. On the basis of the results a ternary phase diagram of the morphologies is mapped. By calcination, anatase TiO2 films are achieved. The morphologies and crystallographic phase of the films are studied with AFM, SEM, and XRD, respectively, and the formation mechanisms of the different morphologies are discussed.
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PMID:Morphology phase diagram of ultrathin anatase TiO2 films templated by a single PS-b-PEO block copolymer. 1659 3

Patterning in the intensively evaporated polymer solutions based on polystyrene and poor solvent (acetone) was investigated. SEM and AFM studies demonstrated that annular elements of the surface topography are formed in this case, in contrast to the honeycomb patterns obtained under the evaporation of the good solvent (chloroform). The authors suggest that the theory of viscous dewetting developed by de Gennes explains the phenomenon satisfactorily.
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PMID:Patterning in rapidly evaporated polymer solutions: formation of annular structures under evaporation of the poor solvent. 1662 28

Factors affecting filtration characteristics in submerged hollow fiber membrane were investigated in membrane-coupled moving bed biofilm reactor (M-CMBBR). The trend of membrane biofouling in M-CMBBR was quite different from that in a conventional membrane bioreactor (MBR). The M-CMBBR showed much lower biofouling rate than a conventional MBR. Whereas the membrane biofouling in conventional MBR system is known to be dependent mostly on biochemical effects of mixed liquor (soluble COD, EPS, etc.), the extent of biofouling in M-CMBBR was largely dependent on the potential collision energy of biofilm carriers (media) moving freely and colliding with surfaces of submerged hollow fibers. The collisions between circulating media and hollow fiber membranes gave rise to frictional forces which mitigated the formation of biofilms on the outer surface of hollow fibers. Consequently, the membrane permeability was greatly enhanced. The potential collision energy of moving media was dependent on the media volume fraction as well as the air flow rate. The membrane permeability was found to be proportional to the relative potential collision energy of the biofilm carriers. The frictional effect on the morphology of biofilms formed on the surface of organic membrane under various operating condition was also examined and identified through their visualization with SEM and AFM.
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PMID:Factors affecting filtration characteristics in membrane-coupled moving bed biofilm reactor. 1663 Dec 28

A novel proton conductor has been realized by employing a ternary polymer blend system in combination with an electric-field orientation technique. A polymer film recast from a solution containing poly(acrylic acid), poly(vinyl butyral), and fluoroalkyl graft polymer under 2 kV.cm(-1) exhibited 10 times higher proton conductivity than that prepared without the external electric field. However, when the film was prepared under a field higher than 4 kV.cm(-1), proton conductivity decreased. The membranous character has been investigated by SEM and AFM observations. As a result, it has been proven that an electric-field treatment of 2 kV.cm(-1) forms the largest hydrophilic domains for proton conduction in the film. The alteration of the phase separation morphology induced by the electric field well explains the proton conductivity change.
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PMID:Electric-field oriented polymer blend film for proton conduction. 1664 51

Effect of side-chain substitutions on the morphology of self-assembly of perylene diimide molecules has been studied with two derivatives modified with distinctly different side-chains, N,N'-di(dodecyl)-perylene-3,4,9,10-tetracarboxylic diimide (DD-PTCDI) and N,N'-di(nonyldecyl)-perylene-3,4,9,10-tetracarboxylic diimide (ND-PTCDI). Due to the different side-chain interference, the self-assembly of the two molecules results in totally different morphologies in aggregate: one-dimensional (1D) nanobelt vs zero-dimensional (0D) nanoparticle. The size, shape, and topography of the self-assemblies were extensively characterized by a variety of microscopies including SEM, TEM, AFM, and fluorescence microscopy. The distinct morphologies of self-assembly have been obtained from both the solution-based processing and surface-supported solvent-vapor annealing. The nanobelts of DD-PTCDI fabricated in solution can feasibly be transferred to both polar (e.g., glass) and nonpolar (e.g., carbon) surfaces, implying the high stability of the molecular assembly (due to the strong pi-pi stacking). The side-chain-dependent molecular interaction was comparatively investigated using various spectrometries including UV-vis absorption, fluorescence, X-ray diffraction, and differential scanning calorimetry. Compared to the emission of ND-PTCDI aggregate, the emission of DD-PTCDI aggregate was significantly red-shifted (ca. 30 nm) and the emission quantum yield decreased about three times, primarily due to the more favorable molecular stacking for DD-PTCID. Moreover, the aggregate of DD-PTCDI shows a pronounced absorption band at the longer wavelength, whereas the absorption of ND-PTCDI aggregate is not significant in the same wavelength region. These optical spectral observations are reminiscent of the previous theoretical investigation on the side-chain-modulated electronic properties of PTCDI assembly.
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PMID:Effect of side-chain substituents on self-assembly of perylene diimide molecules: morphology control. 1673 95

Thermolysis of [M(SeCH2CH2CH2NMe2)2] (M = Zn, Cd, Hg), prepared by the reactions of sodium salt of 3-(N,N-dimethylamino)propaneselenolate with metal acetates, afforded metal selenides (MSe). The metal selenides were characterized by XRD, EDAX, SEM, AFM, and TEM techniques. Nanoparticles of HgSe were prepared by pyrolysis in a quartz boat, solvothermal, and sonochemical methods. EDAX showed 1:1 Hg/Se ratio, while XRD and SAED patterns confirmed the formation of cubic HgSe. These particles are spherical in nature with an average diameter of 15 nm (from TEM).
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PMID:Synthesis and characterization of metal selenide (ZnSe, CdSe, HgSe) nanoparticles. 1673 62

We investigated the potential of commercially available porous templates to be used for the fabrication of functional anisotropic conductors. A galvanostatic deposition technique was used to fabricate arrays consisting of 200 nm diameter nanowires inside the pores of polycarbonate membranes. A tape lift-off procedure allowed the complete removal of any residual metal from both sides of the polymer membrane to form an anisotropic conductive film. The 10 microm thick film has roughly 3 x 10(8) nanowires per cm2, and it showed near zero electrical resistance perpendicular to the surface while appearing completely open to circuits between any points on the surface. The preparation of the film, characterization using SEM, AFM, and resistance measurements are presented. The 1D conductivity of these membranes may have many potential applications for microelectronic interconnects for packaging technologies.
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PMID:Synthesis and characterization of nanowire-based anisotropic conductors. 1673 77

A novel synthetic approach to biodegradable amphiphilic copolymers based on poly (epsilon-caprolactone) (PCL) and chitosan was presented, and the prepared copolymers were used to prepare nanoparticles successfully. The PCL-graft-chitosan copolymers were synthesized by coupling the hydroxyl end-groups on preformed PCL chains and the amino groups present on 6-O-triphenylmethyl chitosan and by removing the protective 6-O-triphenylmethyl groups in acidic aqueous solution. The PCL content in the copolymers can be controlled in the range of 10-90 wt %. The graft copolymers were thoroughly characterized by 1H NMR, 13C NMR, FT-IR and DSC. The nanoparticles made from the graft copolymers were investigated by 1H NMR, DLS, AFM and SEM measurements. It was found that the copolymers could form spherical or elliptic nanoparticles in water. The amount of available primary amines on the surface of the prepared nanoparticles was evaluated by ninhydrin assay, and it can be controlled by the grafting degree of PCL.
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PMID:Synthesis and characterization of the biodegradable polycaprolactone-graft-chitosan amphiphilic copolymers. 1676 Dec 62

A novel biologically relevant composite substrate has been prepared consisting of a calcium phosphate (CaP) layer formed by magnetron sputter-coating from a hydroxyapatite (HA) target onto a gold-coated silicon substrate. The CaP layer is intended to mimic tooth and bone surfaces and allows polymers used in oral care to be deposited in a procedure analogous to that used for dental surfaces. The polymer cetyl dimethicone copolyol (CDC) was deposited onto the CaP surface of the substrate by Langmuir Blodgett deposition, and the structure of the adsorbed layer was investigated by the surface specific technique of sum frequency generation (SFG) vibrational spectroscopy. The gold sublayer provides enhancement of the SFG signal arising from the polymer but plays no part in the adsorption of the polymer. The surface morphology of the substrate was investigated using SEM and AFM. The surface roughness was commensurate with that of the thermally evaporated gold sublayer and uniform over areas of at least 36 mum(2). The chemical composition of the CaP-coated surface was determined by FTIR and TOF-SIMS. It was concluded that the surface is primarily calcium phosphate present as a mixture of amorphous, non-hydroxylated phases rather than solely stoichiometric hydroxyapatite. The SFG spectra from CDC on CaP were closely similar, both in resonance wavenumbers and in their relative intensities, with spectra of thin films of CDC recorded directly on gold. Application of previous analysis of the spectra of CDC on gold therefore enabled interpretation of the polymer orientation and conformation on the CaP substrate.
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PMID:Development of a biologically relevant calcium phosphate substrate for sum frequency generation vibrational spectroscopy. 1683 76

Binary colloidal crystals (BCCs) were prepared from two kinds of poly(styrene-methyl methacrylate-acrylic acid) colloids approximately 190 and approximately 380 nm in diameter by the codeposition method. A variety of array patterns of BCCs were observed and characterized by AFM and SEM. The significance of these colloidal arrays in crystallography has been discussed preliminarily.
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PMID:Array patterns of binary colloidal crystals. 1685 Nov 45


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