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231.
Chalcogenide glass fibers based on sulphide, selenide, telluride, and their rare earth doped compositions are being actively pursued both at the Naval Research Laboratory in Washington, D.C. (NRL) and worldwide. Great strides have been made in reducing optical losses using improved chem ical purification techniques, but further improvements are needed in both purification and fiberization technology to attain the theoretical optical losses. Despite this, current singlemode and multimode chalcogenide glass fibers are enabling numerous applications. Some of these applications include laser power delivery, chemical sensing, imaging, scanning near field microscopy spectroscopy, fiber infrared (IR) sources lasers, amplifiers, and optical switches. The authors assert that the research and development of chalcogenide glasses will grow in the foreseeable future, especially with respect to improvements the optical quality of the fibers and the performance of the fibers in existing future applications.  相似文献   
232.
We report a new method for the direct labeling and visualization of crystalline cellulose using quantum dots (QDs) directed by carbohydrate-binding modules (CBMs). Two type-I (surface binding) CBMs belonging to families 2 and 3a were cloned and expressed with dual histidine tags at the N- and C-termini. Semiconductor (CdSe)ZnS QDs were used to label these CBMs following their binding to Valonia cellulose crystals. Using this approach, we demonstrated that QDs are linearly arrayed on cellulose, which implies that these CBMs specifically bind to a planar face of cellulose. Direct imaging has further shown that different sizes (colors) of QDs can be used to label CBMs bound to cellulose. Furthermore, the binding density of QDs arrayed on cellulose was modified predictably by selecting from various combinations of CBMs and QDs of known dimensions. This approach should be useful for labeling and imaging cellulose-containing materials precisely at the molecular scale, thereby supporting studies of the molecular mechanisms of lignocellulose conversion for biofuels production.  相似文献   
233.
This paper is the first report about the morphology of semi-crystalline poly(ε-caprolactone) (PCL) brushes studied by Atomic Force Microscopy (AFM) in tapping mode. This represents a convenient way to observe how the growth of a polymer proceeds from a thiol monolayer on gold substrate in terms of grafting density and thiol monolayer stability. The synthesis of semi-crystalline PCL brushes was carried out by Ring-Opening Polymerization (ROP) of ε-caprolactone (ε-CL) from hydroxyl end-group of thiol monolayer on gold surface as catalyzed with tin octoate (Sn(Oct)2) at 50 °C. Addition of a sacrificial initiator was also attempted in order to get a finer control over PCL crystals. For a sake of comparison, triazabicyclo[4.4.0]dec-5-ene (TBD) was also investigated as another ROP catalyst active at ambient temperature. The composition and the morphology of resulting semi-crystalline PCL brushes were characterized using X-ray Photoelectron Spectroscopy (XPS) and AFM. In the case of Sn(Oct)2-promoted ROP of CL with or without free (sacrificial) initiator (i.e., benzyl alcohol), different types of morphologies were observed on the gold substrate, due to the thermal instability of thiol-gold bond under the experimental conditions. When TBD was used at ambient temperature, a regular and homogeneous crystalline morphology, i.e., compact PCL crystals, could be observed.  相似文献   
234.
Surface interpenetrating network (IPN) polymers are emerging hybrid materials in which the surface of existing polymers can be modified to preserve their chemical structure and bulk properties. A detailed structural characterization of poly(ethylene terephthalate) (PET) thin films on nanoscopically flat silicon wafers has been carried out by Scanning Probe Microscopy (SPM) and X-ray photoelectron spectroscopy (XPS). Examination of the surface of spin-coated annealed PET film by the SPM in tapping mode revealed a two-phase structure. One phase appeared as a dense crystalline fraction of the polymer while the other was identified as amorphous. These findings were supported by Differential Scanning Calorimetry (DSC), which recognized the crystallinity of annealed PET film at 30%. Modification of the PET surface with interpenetrating polyacrylamide (PAM) increased the roughness of the surface with uniform properties. The depth profiling with XPS revealed that PAM interpenetration extended down to 7.2 nm, confirming a three-dimensional character of the polymer modification, with a relative mass concentration of PAM at about 30.7% in the IPN interface.  相似文献   
235.
Focused by a high numerical-aperture objective in free space, the cylindrical vector beam phase-encoded by vortex phase plate with higher topological charge was capable to generate the doughnut-shaped spot in the vicinity of the focal region. The width of the dark focal spot was manipulated by the phase plate with different topological charge. The relationship between the properties of the focal spot and the vortex phase plate was explicitly analyzed for the input beam with different cylindrical vector polarization. Furthermore, the experimental verification was undertaken at the incidence beam λ = 635 nm with the radial and azimuthal polarization. The experimental results are in excellent agreement with the theoretical calculation.  相似文献   
236.
One-dimensional (1D) nanostructures of fused ring polymeric systems: polyindene (PIn) and polyindole (PInd) were fabricated onto glass substrates using a chemical vapor deposition (CVD) method. Morphology of fabricated PIn and PInd structures studied using Olympus microscope reveals formation of 1D straight tubular, smooth and fluorescent nanostructures. The results obtained were further correlated with scanning electron microscopic (SEM) studies of PIn and PInd nanostructures, indicating appearance of fine nanothread entangled network (having diameter ∼ 50 nm) for PIn, and well-defined, straight and aligned nanotubes (having diameter ∼ 60 nm) for PInd. A comparative study on the morphology/dimensions of fabricated PIn and PInd nanostructures with the nanosized PIn and PInd structures obtained by oxidative synthetic routes is also discussed. The structural composition of fabricated PIn and PInd nanostructures is confirmed by Fourier transform infrared (FTIR) spectroscopy, thereby indicating existence of all infrared markers corresponding to the characteristic bands present in PIn and PInd. The study suggests that the fabricated PIn and PInd nanodimensional structures may find potential applications in the field of nanotechnology.  相似文献   
237.
生物医学光声成像的研究进展   总被引:2,自引:2,他引:0       下载免费PDF全文
陶超  刘晓峻 《应用声学》2012,31(6):401-409
光声成像是21世纪初发展起来的新兴的生物医学成像技术,它同时具备光学成像和声学成像两者的优点,因而备受关注。本文对生物医学光声成像的发展进行了综述。首先,介绍了光声成像的特点以及相对于广泛应用的光学成像技术和声学成像技术的优点;其次,在成像原理上解释了光声成像优点的成因,并介绍了光声断层成像和光声显微镜这两种典型的光声成像技术;再次,详细介绍了多尺度的光声图像分辨率和成像深度,以及多信息维度的光声成像参数;最后,展望了光声成像在生物医学领域的应用潜力并讨论了其局限性。  相似文献   
238.
The miscibility of polycarbonate (PC) with poly(methyl methacrylate-co-cyclohexyl methacrylate) (PMCHM) and with poly(methyl methacrylate) (PMMA) was studied by nuclear magnetic resonance (NMR) 1H spin-lattice relaxation time in the rotating frame (1H T1p), differential scanning calorimetry (DSC), and transmission electron microscopy (TEM). A blend of PC/PMCHM (50/50 wt/wt) with the acrylic component PMCHM, a copolymer of PMMA and poly(cyclohexyl methacrylate) (80/20 wt/wt), shows only one T1p value, which indicates high miscibility in this blend. A blend of PC/PMMA (50/50 wt/wt) shows two 1H T1p values, which are similar to those of the homopolymers PC and PMMA. These results indicate high immiscibility. The “domain size” calculated from NMR results of the miscible blend PC/PMCHM is approximately 40 Å. The results of DSC and TEM are similar to the NMR results. However, TEM results show the presence of 3% PC domains in the PC/PMCHM blend, which are not seen by NMR or DSC. Those PC domains are approximately 500 Å. A strong intramolecular repulsion in the copolymer PMCHM and specific intermolecular interactions between PC and PMMA may explain the miscibility in the PC/PMCHM system. © 1994 John Wiley & Sons, Inc.  相似文献   
239.
The laccase enzymes of Agaricus bisporus and Trametes versicolor were successfully covalently co-immobilized on poly(glycidyl methacrylate) microspheres. The enzyme load reached after the co-immobilization of both enzymes was 6.75 U g−1 carrier. The resulting biocatalyst showed the combined properties of both immobilized enzymes, increasing their optimum pH and temperature ranges. The storage and operational stabilities were also improved after co-immobilization. In presence of mediator (ABTS) the organophosphate pesticide diazinon was 100% biodegraded after 48 h of reaction with 0.2 U/mL of co-immobilized enzymes (at the two maximum activity pH values: 2.0 and 3.0). In the absence of a mediator, the degradation percentages were above 88%. Data showed that, compared with single enzymatic immobilization, the co-immobilization of the two laccases is an easy, efficient, and low cost alternative to expanding the range of work of the biocatalyst, thereby improving the stability and some biochemical properties to generate a powerful alternative for pesticide degradation in a wide range of conditions.  相似文献   
240.
《European Polymer Journal》2004,40(1):211-217
Continuous and discontinuous gold layers sputtered on polyethyleneterephthalate (PET) were characterized using atomic force microscopy (AFM), scanning electron microscopy (SEM) and by reflection of microwave radiation. The changes in the surface morphology of the continuous and discontinuous gold layers as a function of the sputtering time were clearly observed by AFM technique. SEM imaging of very thin gold layers was adversely affected by specimen charging. For medium sputtering times, when a continuous gold coverage is already formed, the SEM technique still show the presence of regions with very thin gold coverage which gradually disappear at longer sputtering times. Both, the AFM and SEM techniques confirmed that in the course of the gold deposition the initially small gold clusters grow and finally associate in a continuous layer. It was shown that the sub-microne metallic structures could be modeled by artificial, significantly larger structures prepared on PET by lithographic etching.  相似文献   
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