Gene/Protein Disease Symptom Drug Enzyme Compound
Pivot Concepts:   Target Concepts:
Query: UMLS:C0276640 (TEM)
 20,729 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Double-surface-silvered polyimide films have been successfully fabricated using silver ammonia complex cation ([Ag(NH3)2]+) as the silver precursor and 3,3',4,4'-benzophenonetetracarboxylic dianhydride/4,4'-oxidianile- (BTDA/ODA-) based poly(amic acid) (PAA) as the polyimide precursor via a direct ion-exchange self-metallization technique. The process has been clarified to involve the loading of silver(I) into PAA via ion exchange, the thermally induced reduction of silver(I) to silver(0) and the concomitant imidization of PAA to polyimide upon thermal treatment, the subsequent silver-catalyzed and oxygen-assisted decomposition of the polyimide overlayer, and the self-accelerated aggregation of silver clusters on the film surface to produce well-defined surface silver layers. By employing [Ag(NH3)2]+ solution with a concentration of only 0.01 M and an ion-exchange time of no more than 10 min, the controlled formation of highly reflective and conductive silver surfaces upon thermal treatment at 300 degrees C for less than 4.5 h indicates that the present work provides an efficient route and an effacious silver species for polyimide surface metallization. Although the alkaline characteristics of [Ag(NH3)2]+ have a strong hydrolysis effect on the polyimide precursor chains, the final metallized films retain the key mechanical and thermal properties of the pure polyimide. Films were characterized by ATR-FTIR, XPS, ICP-AES, SEM, TEM, DSC, TGA, reflectivity, conductivity, and mechanical measurements.
 ...
PMID:Controlled formation of optically reflective and electrically conductive silvered surfaces on polyimide film via a direct ion-exchange self-metallization technique using silver ammonia complex cation as the precursor. 1840 10

In a previous work, we studied the interaction of beta-amyloid fibrils (Abeta) with gold nanoparticles (AuNP) conjugated with the peptide CLPFFD-NH2. Here, we studied the effect of changing the residue sequence of the peptide CLPFFD-NH2 on the efficiency of conjugation to AuNP, the stability of the conjugates, and the affinity of the conjugates to the Abeta fibrils. We conjugated the AuNP with CLPFFD-NH 2 isomeric peptides (CDLPFF-NH2 and CLPDFF-NH2) and characterized the resulting conjugates with different techniques including UV-Vis, TEM, EELS, XPS, analysis of amino acids, agarose gel electrophoresis, and CD. In addition, we determined the proportion of AuNP bonded to the Abeta fibrils by ICP-MS. AuNP-CLPFFD-NH2 was the most stable of the conjugates and presented more affinity for Abeta fibrils with respect to the other conjugates and bare AuNP. These findings help to better understand the way peptide sequences affect conjugation and stability of AuNP and their interaction with Abeta fibrils. The peptide sequence, the steric effects, and the charge and disposition of hydrophilic and hydrophobic residues are crucial parameters when considering the design of AuNP peptide conjugates for biomedical applications.
 ...
PMID:How changes in the sequence of the peptide CLPFFD-NH2 can modify the conjugation and stability of gold nanoparticles and their affinity for beta-amyloid fibrils. 1851 Mar 52

Formations of Y and T nano junctions have been observed in boron nitride films deposited on silicon substrates by plasma chemical reaction of diborane (B2H6 diluted in hydrogen) and ammonia (NH3) gases using dual frequency (microwave/radio) plasma enhanced chemical vapor deposition technique without any intentional heating of the substrates. It has been observed that these nano junctions form at a critical feed gas ratio of ammonia and diborane. We have investigated the effect of gas feed ratio R (=NH3/B2H6) in the plasma reaction chamber, keeping all other deposition parameters constant, on the morphology of boron nitride films. The deposited films are characterized by SEM, AFM, TEM and Laser Raman. For gas feed ratio, R < 100, octahedron and cubic morphologies have been observed in BN films and on increasing R to >100, size of the crystallites reduces to nanometer level. In some of our BN samples deposited at a critical value of gas ratio (R = 400), uniform Y and T junctions having bamboo like morphologies, in nanometer level, have been observed, which we wish to emphasis here as an interesting and newer observation in boron nitride films deposited by the dual frequency PECVD technique. This change in morphology exhibited by varying gas feed ratio is mainly due to excess nitrogen ions in the plasma.
 ...
PMID:Morphological observation of Y and T junctions in nanostructured boron nitride thin films. 1905 6

Biologically derived materials provide a rich variety of approaches toward new functional materials because of their fascinating structures and environment-friendly features, which is currently a topic of research interest. In this paper, we show that the cuttlebone-derived organic matrix (CDOM) is an excellent scaffold for the one-step synthesis and assembly of silver nanoparticles (AgNPs), which can be further used as substrate for surface-enhanced Raman scattering (SERS). Formation of AgNPs-CDOM composite was accomplished by the reaction of CDOM with AgNO(3) and NH(3).H(2)O solution at 80 degrees C without using any other stabilizer and reducing agents. UV-vis spectra and TEM were utilized to characterize the AgNPs and investigate their formation process. Results demonstrate that the size and distribution of AgNPs can be partly regulated by changing incubation time; the concentration of NH(3).H(2)O is critical to the formation rate of AgNPs. As a proof of principle, we show that the AgNPs-CDOM composite can be employed in trace analysis using SERS.
 ...
PMID:Cuttlebone-derived organic matrix as a scaffold for assembly of silver nanoparticles and application of the composite films in surface-enhanced Raman scattering. 1909 22

Yellowish (Fe, N)-doped nanocrystalline TiO2 powders have been prepared using TiOSO4, CO(NH2)2, Fe(NO3)3.9H2O and CN3H5.HCl as precursors by hydrothermal method. The as-synthesized powders were anatase in phase and the grain size was about 10 nm according to the TEM photos. The ratio of Fe/Ti is 2.2 at% and N/O is 0.8 at% respectively. TiO2 powders were mixed with organic silicon and acrylic syrup to test their antibacterial performance by the colony counting method. The results show that the sterilization ratio of E. coli by the heat-treated (Fe, N)-doped nanocrystalline TiO2 powders is reached up to 94.5% while that of the powders without any heat treatment is 91.1% by 8 hours-400 lux-Visible-light irradiation with humidity of 55% RH.
 ...
PMID:Preparation of (Fe, N)-doped TiO2 powders and their antibacterial activities under visible light irradiation. 1944 63

Amine monofunctional gold nanoparticles (1-AuNPs) were synthesized by employing a solid-supported technique and pH-switchable pseudorotaxane formation. Purification was repeatedly facilitated using crown ether peripherally coated superparamagnetic iron oxide microspheres to yield the monofunctional gold nanoparticles in excellent yield. The product and its related intermediate superstructures were characterized by IR and X-ray photoelectron spectroscopies. Novel supramolecular dimers and trimers were prepared by titrating the 1-AuNPs with bisDB24C8 and trisDB24C8 at different ratios. UV/visible absorption spectroscopic analyses of the supramolecular dimer and trimer solutions, which were formed by mixing their separate components in different ratios, indicated the gradual appearance of two distinct plasmonic resonance bands at 620 and approximately 700 nm. Furthermore, TEM images of the dimers revealed a significant amount of dimer pairs on the surface, while the TEM images of the trimers demonstrated the presence of both dimers and trimers. The trimers appeared as triangular or near-linear shapes.
 ...
PMID:Discrete functional gold nanoparticles: hydrogen bond-assisted synthesis, magnetic purification, supramolecular dimer and trimer formation. 1962 79

Photoluminescence (PL) and time-resolved PL experiments as a function of the elaboration process are performed on Er-doped silicon-rich silicon oxide (SRO:Er) thin films grown under NH(3) atmosphere. These PL measurements of the Er(3+) emission at 1.54 microm under non-resonant pumping with the Er f-f transitions are obtained for different Er(3+) concentrations, ranging from 0.05 to 1.4 at.%, and various post-growth annealing temperatures of the layers. High resolution transmission electron microscopy (HRTEM) and energy-filtered TEM (EFTEM) analysis show a high density of Si nanostructures composed of amorphous and crystalline nanoclusters varying from 2.7 x 10(18) to 10(18) cm(-3) as a function of the post-growth annealing temperature. Measurements of PL lifetime and effective Er excitation cross section for all the samples under non-resonant optical excitation with the Er(3+) atomic energy levels show that the number of Er(3+) ions sensitized by the silicon-rich matrix decreases as the annealing temperature is increased from 500 to 1050 degrees C. The origin of this effect is attributed to the reduction of the density of sensitizers for Er ions in the SRO matrix when the annealing temperature increases. Finally, extended x-ray absorption fine-structure spectroscopy (EXAFS) shows a strong correlation between the number of emitters and the mean local order around the erbium ions.
 ...
PMID:The evolution of the fraction of Er ions sensitized by Si nanostructures in silicon-rich silicon oxide thin films. 1967 77

In this work, silicon-rich silicon nitride (SRN) layers were deposited on a silicon wafer by microwave-assisted plasma-enhanced chemical vapor deposition (MW-PECVD) using NH(3) and SiH(4) as precursor gases. The Si excess in the as-deposited layers as determined by the Rutherford backscattering technique was controlled by varying the precursor gas ratio. We were able to produce silicon nanoparticles (Si-nps) in the silicon nitride (SiN(x)) layers upon thermal annealing at high temperature. Energy-filtered TEM (EFTEM), complemented by photoluminescence measurements, were used to identify the experimental parameters in order to reach a high density of well-separated Si-nps (3 nm). Our results show that the MW-PECVD method is a suitable deposition tool for the formation of Si-nps in thin SRN layers.
 ...
PMID:Properties of silicon nanoparticles embedded in SiNx deposited by microwave-PECVD. 1976 38

The effects of the addition of three different organosiloxanes, 3-aminopropyltrimethoxysilane (APTMS), 3-aminopropyltriethoxysilane (APTES) and 3-mercaptopropyltrimethoxysilane (MPTMS), on the phase behavior and the pore size of the surfactant-extracted materials have been investigated using powder XRD, TEM, Nitrogen adsorption/desorption isotherms and elemental analysis. The organosiloxanes were added to a typical synthesis, which results in a KIT-6 type in the absence of organosiloxanes. Their addition resulted in mesophase transformation or not, depending on the nature of functional groups of organosiloxanes. Increasing the content of APTMS or APTES in the silica sources not only led to the transformation of mesostructures from cubic bicontinuous Ia-3d to mixed mesostructure then towards two-dimensional (2-D) hexagonal p6mm and eventually to disordered structure, but also caused an increase of the pore size. However, the d spacing and the pore size of the cubic bicontinuous Ia-3d mesoporous solids can be decreased by addition of MPTMS between 0 and 2.5 mol% in the silica sources without a distinct decrease in the long-range order of the material. These results are discussed in terms of differences in the ability of the organosiloxanes to interact with the surfactant P123. The potential applications of these mesoporous materials are supports for the immobilization of enzymes, heavy metal sorbents, base catalysts, etc.
 ...
PMID:Influence of organosiloxanes on the properties of mesoporous materials. 1990 93

A new microporous organic-inorganic hybrid organosilica LHMM-2 containing a bis(propyliminomethyl)benzene moiety inside the framework has been synthesized hydrothermally without using any template or structure-directing agent. Powder XRD and TEM image analyses suggest a new disordered microporous structure with pores of dimension ca. 0.54 nm, and (13)C and (29)Si MAS NMR and spectroscopic results indicate the presence of bridging organic bis(propyliminomethyl)benzene moiety in this framework. TPD-NH(3) results suggested that nearly 5 times as much bis(propyliminomethyl)benzene moiety is located inside the micropore walls (matrix) than in the surface of the pores. LHMM-2 shows very high adsorption capacity for metal cations like Fe(3+), Cu(2+) and Zn(2+).
 ...
PMID:New organic-inorganic hybrid microporous organosilica having high metal ion adsorption capacity. 2061 68


<< Previous 1 2 3 4 5 6 7 8 9 10 Next >>