Numerous Applications (numerous + application)

Distribution by Scientific Domains


Selected Abstracts


Historical review of sample preparation for chromatographic bioanalysis: pros and cons

DRUG DEVELOPMENT RESEARCH, Issue 3 2007
Min S. Chang
Abstract Sample preparation is a major task in a regulated bioanalytical laboratory. The sample preparation procedure significantly impacts assay throughput, data quality, analysis cost, and employee satisfaction. Therefore, selecting and optimizing an appropriate sample preparation method is essential for successful method development. Because of our recent expertise, this article is focused on sample preparation for high-performance liquid chromatography with mass spectrometric detection. Liquid chromatography with mass spectrometric detection (LC-MS) is the most common detection technique for small molecules used in regulated bioanalytical laboratories. The sample preparation technologies discussed are pre-extraction and post-extraction sample processing, protein precipitation (PPT), liquid,liquid extraction (LLE), offline solid-phase extraction (SPE), and online solid-phase extraction. Since all these techniques were in use for more than two decades, numerous applications and variations exist for each technique. We will not attempt to categorize each variation. Rather, the development history, a brief theoretical background, and selected references are presented. The strengths and the limitations of each method are discussed, including the throughput improvement potential. If available, illustrations from presentations at various meetings by our laboratory are used to clarify our opinion. Drug Dev Res 68:107,133, 2007. ©2007 Wiley-Liss, Inc. [source]


Diffusion in Nanocrystalline Metals and Alloys,A Status Report,

ADVANCED ENGINEERING MATERIALS, Issue 5 2003
R. Würschum
Abstract Diffusion is a key property determining the suitability of nanocrystalline materials for use in numerous applications, and it is crucial to the assessment of the extent to which the interfaces in nanocrystalline samples differ from conventional grain boundaries. The present article offers an overview of diffusion in nanocrystalline metals and alloys. Emphasis is placed on the interfacial characteristics that affect diffusion in nanocrystalline materials, such as structural relaxation, grain growth, porosity, and the specific type of interface. In addition, the influence of intergranular amorphous phases and intergranular melting on diffusion is addressed, and the atomistic simulation of GB structures and diffusion is briefly summarized. On the basis of the available diffusion data, the diffusion-mediated processes of deformation and induced magnetic anisotropy are discussed. [source]


Colloidal Films That Mimic Cilia

ADVANCED FUNCTIONAL MATERIALS, Issue 18 2010
Fang Liu
Abstract Cilia are wavy hair-like structures that extend outward from surfaces of various organisms. They are classified into two general categories, primary cilia, which exhibit sensing attributes, and motile cilia, which exert mechanical forces. A new poly(2-(N,N -dimethylamino)ethyl methacrylate- co -n-butyl acrylate- co - N,N -(dimethylamino) azobenzene acrylamide) (p(DMAEMA/nBA/DMAAZOAm) copolymer is prepared using colloidal synthesis, which, upon coalescence, form films capable of generating surfaces with cilia-like features. While film morphological features allow the formation of wavy whiskers, the chemical composition of the copolymer facilitates chemical, thermal, and electromagnetic responses manifested by simultaneous shape and color changes as well as excitation wavelength dependent fluorescence. These studies demonstrate that synthetically produced polymeric films can exhibit combined thermal, chemical, and electromagnetic sensing leading to locomotive and color responses, which may find numerous applications in sensing devices, intelligent actuators, defensive mechanisms, and others. [source]


Large-Scale Synthesis of Long Crystalline Cu2-xSe Nanowire Bundles by Water-Evaporation-Induced Self-Assembly and Their Application in Gas Sensing

ADVANCED FUNCTIONAL MATERIALS, Issue 11 2009
Jun Xu
Abstract By a facile water evaporation process without adding any directing agent, Cu2-xSe nanowire bundles with diameters of 100,300,nm and lengths up to hundreds of micrometers, which comprise crystalline nanowires with diameters of 5,8,nm, are obtained. Experiments reveal the initial formation/stacking of CuSe nanoplates and the subsequent transformation to the Cu2-xSe nanowire bundles. A water-evaporation-induced self-assembly (WEISA) mechanism is proposed, which highlights the driving force of evaporation in promoting the nanoplate stacking, CuSe-to-Cu2-xSe transformation and the growth/bundling of the Cu2-xSe nanowires. The simplicity, benignancy, scalability, and high-yield of the synthesis of this important nanowire material herald its numerous applications. As one example, the use of the Cu2-xSe nanowire bundles as a photoluminescence-type sensor of humidity is demonstrated, which shows good sensitivity, ideal linearity, quick response/recovery and long lifetime in a very wide humidity range at room temperature. [source]


Oligonucleotides Containing 7-Deaza-2,-deoxyinosine as Universal Nucleoside: Synthesis of 7-Halogenated and 7-Alkynylated Derivatives, Ambiguous Base Pairing, and Dye Functionalization by the Alkyne,Azide ,Click' Reaction

HELVETICA CHIMICA ACTA, Issue 7 2008
Frank Seela
Abstract Oligonucleotides containing 7-deaza-2,-deoxyinosine derivatives bearing 7-halogen substituents or 7-alkynyl groups were prepared. For this, the phosphoramidites 2b,2g containing 7-substituted 7-deaza-2,-deoxyinosine analogues 1b,1g were synthesized (Scheme,2). Hybridization experiments with modified oligonucleotides demonstrate that all 2,-deoxyinosine derivatives show ambiguous base pairing, as 2,-deoxyinosine does. The duplex stability decreases in the order Cd>Ad>Td>Gd when 2b,2g pair with these canonical nucleosides (Table,6). The self-complementary duplexes 5,-d(F7c7I-C)6, d(Br7c7I-C)6, and d(I7c7I-C)6 are more stable than the parent duplex d(c7I-C)6 (Table,7). An oligonucleotide containing the octa-1,7-diyn-1-yl derivative 1g, i.e., 27, was functionalized with the nonfluorescent 3-azido-7-hydroxycoumarin (28) by the Huisgen,Sharpless,Meldal cycloaddition ,click' reaction to afford the highly fluorescent oligonucleotide conjugate 29 (Scheme,3). Consequently, oligonucleotides incorporating the derivative 1g bearing a terminal CC bond show a number of favorable properties: i) it is possible to activate them by labeling with reporter molecules employing the ,click' chemistry. ii) Space demanding residues introduced in the 7-position of the 7-deazapurine base does not interfere with duplex structure and stability (Table,8). iii) The ambiguous pairing character of the nucleobase makes them universal probes for numerous applications in oligonucleotide chemistry, molecular biology, and nanobiotechnology. [source]


Forming Highly Ordered Arrays of Functionalized Polymer Nanowires by Dewetting on Micropillars,

ADVANCED MATERIALS, Issue 9 2007
J. Guan
1D nanostructures are of great interest for numerous applications: a simple and low-cost process to generate large arrays of polymer nanowires by dewetting aqueous polymer solution on an array of micropillars is developed. These nanowires are typically less than 10,nm in lateral size and can be functionalized by incorporation of molecules or nanoparticles such as quantum dots (see figure). [source]


How light gets through periodically nanostructured metal films: a role of surface polaritonic crystals

JOURNAL OF MICROSCOPY, Issue 3 2003
A. V. Zayats
Summary The physical origin of the enhanced optical transmission of periodically structured films related to surface plasmon polaritons is discussed from first principles. The enhancement of transmission through smooth, randomly rough and periodically nanostructured films is considered. Analysis shows that any metal (or dielectric) nanostructured film can exhibit enhanced transmission in certain spectral ranges corresponding to surface plasmon (or phonon) polariton Bloch mode states on a periodic structure. Resonant tunnelling via these states is responsible for the transmission enhancement. The properties of surface polaritonic crystals are analogous to those of photonic crystals and can find numerous applications for scaling down optical devices to nanometric dimensions as well as for designing novel nanostructured materials whose optical properties are determined by surface polariton interaction in a periodic structure. [source]


Optical properties of correlated materials , Or why intelligent windows may look dirty,

PHYSICA STATUS SOLIDI (B) BASIC SOLID STATE PHYSICS, Issue 9 2009
Jan M. Tomczak
Abstract Materials with strong electronic Coulomb correlations play an increasing role in modern materials applications. "Thermochromic" systems, which exhibit thermally induced changes in their optical response, provide a particularly interesting case. The optical switching associated with the metal,insulator transition of vanadium dioxide (VO2), for example, has been proposed for use in numerous applications, ranging from anti-laser shields to "intelligent" windows, which selectively filter radiative heat in hot weather conditions. Are present-day electronic structure techniques able to describe, or , eventually even predict , such a kind of behavior? How far are we from materials design using correlated oxides? These are the central questions we try to address in this article. We review recent attempts of calculating optical properties of correlated materials within dynamical mean field theory, and summarize results for VO2 obtained within a novel scheme aiming at particularly simple and efficient calculations of optical transition matrix elements within localized basis sets. Finally, by optimizing the geometry of "intelligent windows," we argue that this kind of technique can, in principle, be used to provide guidance for experiments, thus giving a rather optimistic answer to the above questions. [source]


Analyses of Thick Lithium Coatings Deposited by Sputter-Evaporation and Exposed to Air

PLASMA PROCESSES AND POLYMERS, Issue S1 2009
C. Rigaux
Abstract Lithium coatings on various substrates have numerous applications: Boron neutron capture therapy, neutron activation analysis, super-conducting tokamak etc. Traditionally these coatings are produced by well-known techniques such as electrochemistry and evaporation. In this work, we investigated a new method based on sputter-evaporation, which enables thick coatings (>10,µm) to be built on various substrates within a short timeframe. In order to minimize the process time, evaporation techniques can be used but the coating quality suffers. Moreover, it is well known that the use of DC magnetron sputtering results in the deposition of good quality coatings (smoothness, density, adhesion); however, the deposition rate is low. The rationale of this work is to combine these two techniques, yielding a sputter-evaporation process that possesses the advantages of each separate technique. Li is placed in a stainless steel crucible (cathode), and heated by the plasma generated by a magnetron discharge. The Li temperature is measured by a thermocouple welded onto the cathode and measured at different plasma power densities. The deposition rate of lithium is measured using a quartz balance and by profilometry, at several temperatures (from 0 to 580,°C). Li samples were depth-profiled with the resonant nuclear reaction 7Li(p,,)7. In addition to the concentration, certain characteristics like the density and the chemical reactivity of layers, are also important. Thus we have studied the evolution of the density with time, estimated by weight and profilometry measurements, and the change in morphology, by cross-sectional scanning electron microscopy (SEM), of samples exposed to air at room temperature. The evolution of the film compounds have also been determined by X-ray powder diffraction. These physical properties have been investigated for various bias substrates during deposition. [source]


Multiple neural networks modeling techniques in process control: a review

ASIA-PACIFIC JOURNAL OF CHEMICAL ENGINEERING, Issue 4 2009
Zainal Ahmad
Abstract This paper reviews new techniques to improve neural network model robustness for nonlinear process modeling and control. The focus is on multiple neural networks. Single neural networks have been dominating the neural network ,world'. Despite many advantages that have been mentioned in the literature, some problems that can deteriorate neural network performance such as lack of generalization have been bothering researchers. Driven by this, neural network ,world' evolves and converges toward better representations of the modeled functions that can lead to better generalization and manages to sweep away all the glitches that have shadowed neural network applications. This evolution has lead to a new approach in applying neural networks that is called as multiple neural networks. Just recently, multiple neural networks have been broadly used in numerous applications since their performance is literally better than that of those using single neural networks in representing nonlinear systems. Copyright © 2009 Curtin University of Technology and John Wiley & Sons, Ltd. [source]


Functionalization of Gold and Glass Surfaces with Magnetic Nanoparticles Using Biomolecular Interactions

BIOTECHNOLOGY PROGRESS, Issue 1 2006
Bala G. Nidumolu
Advances in nanotechnology have enabled the production and characterization of magnetic particles with nanometer-sized features that can be functionalized with biological recognition elements for numerous applications in biotechnology. In the present study, the synthesis of and interactions between self-assembled monolayers (SAMs) on gold and glass surfaces and functionalized magnetic nanoparticles have been characterized. Immobilization of 10,15 nm streptavidin-functionalized nanoparticles to biotinylated gold and glass surfaces was achieved by the strong interactions between biotin and streptavidin. Fluorescent streptavidin-functionalized nanoparticles, biotinylated surfaces, and combinations of the two were characterized by Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, and electron and fluorescent microscopy to confirm that little or no functionalization occurred in nonbiotinylated regions of the gold and glass surfaces compared to the biotinylated sites. Together these techniques have potential use in studying the modification and behavior of functionalized nanoparticles on surfaces in biosensing and other applications. [source]


Glycerol Etherification over Highly Active CaO-Based Materials: New Mechanistic Aspects and Related Colloidal Particle Formation

CHEMISTRY - A EUROPEAN JOURNAL, Issue 7 2008
Agnieszka
Abstract Glycerol is an attractive renewable building block for the synthesis of di- and triglycerols, which have numerous applications in the cosmetic and pharmaceutical industries. In this work, the selective etherification of glycerol to di- and triglycerol was studied in the presence of alkaline earth metal oxides and the data are compared with those obtained with Na2CO3 as a homogeneous catalyst. It was found that glycerol conversion increased with increasing catalyst basicity; that is, the conversion increases in the order: MgO90,% at 60,% conversion) are obtained over CaO, SrO, and BaO. For these catalysts no substantial acrolein formation was observed. Furthermore, at the start of the reaction mainly linear diglycerol was produced, whereas at higher conversion degrees branched diglycerol started to form. In another series of experiments different types of CaO materials were prepared. It was found that these CaO-based materials not only differed in their surface area and number of basic sites, but also in their Lewis acid strength. Within this series the CaO material possessing the strongest Lewis acid sites had the highest catalytic activity, comparable to that of BaO, pointing towards the important role of Lewis acidity for this etherification reaction. Based on these observations a plausible alternative reaction scheme for glycerol etherification is presented, which considers the facilitation of the hydroxyl leaving process. Finally, the stability of the catalytic solids under study was investigated and it was found that colloidal CaO particles of about 50,100,nm can be spontaneously generated during reaction. Catalytic testing of these CaO colloids, after isolation from the reaction medium, revealed a very high etherification activity. Understanding the nature of these Ca-based colloids opens new opportunities for investigating supported colloidal particle catalysts to take advantage of both their hetero- and homogeneous nature. [source]


Coming of Age: Sustainable Iron-Catalyzed Cross-Coupling Reactions

CHEMSUSCHEM CHEMISTRY AND SUSTAINABILITY, ENERGY & MATERIALS, Issue 5 2009
Waldemar Maximilian Czaplik
Abstract Iron-catalyzed cross-coupling reactions have, over the past years, developed to maturity and today are an integral part of the organic chemist's toolkit. They benefit from low costs, operational simplicity, and high reactivity and thus constitute the "green" sister of the palladium and nickel establishment. This timely Review traces back major achievements, discusses their mechanistic background, and highlights numerous applications to molecular synthesis. Iron-catalyzed carbon,carbon bond-forming reactions have matured to an indispensable class of reactions in organic synthesis. The advent of economically and ecologically attractive iron catalysts in the past years has stepped up the competition with the established palladium and nickel catalyst systems that have dominated the field for more than 30 years, but suffer from high costs, toxicity, and sometimes low reactivity. Iron-catalyzed protocols do not merely benefit from economic advantages but entertain a rich manifold of reactivity patterns and tolerate various functional groups. The past years have witnessed a rapid development with ever-more-efficient protocols for the cross-coupling between alkyl, alkenyl, alkynyl, aryl, and acyl moieties becoming available to organic chemists. This Review intends to shed light onto the versatility that iron-catalyzed cross-coupling reactions offer, summarize major achievements, and clear the way for further use of such superior methodologies in the synthesis of fine chemicals, bioactive molecules, and materials. [source]