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The dielectric constant, dielectric loss, and ac conductivity of polyblends of cellulose acetate hydrogen phthalate (CAP) and poly (vinyl pyrrolidone) (PVP) of different compositions were measured in the temperature range of 300–430 K and in the frequency range of 50 Hz–100 kHz. In the blends, the dielectric constant as well as the dielectric loss as a function of the temperature display a single peak corresponding to the glass transition temperature (Tg) in the region between the Tg values of the pure polymers. The Tg values observed agree well with those values obtained from DSC. Dielectric studies show that CAP forms a miscible blend with PVP. Ac conductivity values were calculated from the dielectric data and the conduction mechanism is discussed. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 86: 1702–1708, 2002  相似文献   
3.
HgTe/Hg0.05Cd0.95Te superlattices (SLs) were grown on (112)B oriented Cd0.96Zn0.04 Te substrates using molecular beam epitaxy (MBE). The SLs, consisting of 100 periods of 80-Å-thick HgTe wells alternating with 77-Å-thick Hg0.05Cd0.95Te barriers, were designed to operate as detectors in the far-infrared (FIR) region. Infrared absorption spectroscopy, high-resolution transmission electron microscopy (TEM), Hall effect measurements, and x-ray diffraction were used to characterize the superlattice layers. A series of annealing experiments were initiated to quantify the temperature-dependent interdiffusion of the HgTe wells and Hg0.05Cd0.95Te barriers and consequently their degradation, which shifts the absorption edges of the SLs to higher energies, since a high-temperature ex situ anneal is normally required in order to produce the p-type material required for a photovoltaic detector. Results from infrared absorption spectroscopy, TEM, and Hall effect measurements for the annealed samples are presented. A FIR SLs single-element photoconductive (PC) device was designed and fabricated. Both material characterization and device testing have established the applicability of the HgTe/Hg0.05Cd0.95Te SLs for the FIR region.  相似文献   
4.
The effect of paddle element geometry, specifically a systematic change in stagger angle, on the velocity distribution of a Newtonian corn syrup was evaluated in the mixing region of a 2″ Readco continuous processor using 3D FEM simulations. Local velocities and regions of backflow were compared for three configurations of the paddle elements in the mixing region consisting of nine pairs of paddle elements with the central three being in a neutral (FLAT), staggered 45° forward (45F) or staggered 45° reverse (45R) configuration. The total material flow rate through the mixer was independent of the paddle element stagger but increased with screw speed when the mixer was operated with the barrel fully filled. The stagger angle variation caused only local disturbances in axial flow. The overall magnitudes of velocity were highest for the FLAT configuration followed by 45F and 45R. The local X and Y velocity components in the region of stagger showed no significant variation with paddle element stagger while the Z velocity component varied significantly in this region. Increased forward flow was seen for the 45F configuration while significant local backflow was seen for the 45R configuration at all positions of the paddle element rotation. The FLAT configuration had greater levels of pressure in the intermeshing region, suggesting a squeeze flow while there were not significant variations in pressure for the 45F and 45R configurations, suggesting a predominantly conveying/leakage flow in the axial direction. Variation in local flows is critical to good mixing.  相似文献   
5.
In this paper we report the calculated results of the dark current and multiplication factor in MBE grown HgCdTe avalanche photodiodes with separate absorption and multiplication (SAM-APD). The device architecture used for this analysis comprises the following layers: p+ contact, p junction, n multiplication, n charge sheet, n absorber, and n+ contact. Various leakage current mechanisms are considered and the generation-recombination term is found to be the dominant one for this device structure. However, experimental reverse bias I-V characteristics reported earlier by T. de Lyon et al. shows a large deviation from ideality, which can not be explained in terms of bulk leakage current mechanism. To explain the large difference between experimental and theoretical data we consider that the dominant generation-recombination current is multiplied through impact ionization process. To validate this assumption, multiplication is calculated as a function of reverse bias. Electric field profile is obtained and the multiplication is computed using the ionization coefficients and avalanche gain equations. Breakdown voltage is found to be 85 V for room temperature operation in agreement with available data in the literature. The theoretical I-V curves considering multiplication are compared with the experimental ones and a close agreement is found which validate this model.  相似文献   
6.
The morphology of the active layer of a bulk heterojunction solar cell, made of a blend of an electron‐donating polymer and an electron‐accepting fullerene derivative, is known to play a determining role in device performance. Here, a combination of molecular dynamics simulations and long‐range corrected density functional theory calculations is used to elucidate the molecular‐scale effects that even minor structural changes to the polymer backbone can have on the “local” morphology; this study focuses on the extent of polymer–fullerene mixing, on their packing, and on the characteristics of the fullerene–fullerene connecting network in the mixed regions, aspects that are difficult to access experimentally. Three representative polymer donors are investigated: (i) poly[(5,6‐difluoro‐2,1,3‐benzothiadiazol‐4,7‐diyl)‐alt‐(3,3′″‐di(2‐octyldodecyl)‐2,2′;5′,2″;5″,2′″‐quaterthiophen‐5,5′″‐diyl)] (PffBT4T‐2OD); (ii) poly[(2,1,3‐benzothiadiazol‐4,7‐diyl)‐alt‐(3,3′″‐di(2‐octyldodecyl)‐2,2′;5′,2″;5″,2′″‐quaterthiophen‐5,5′″‐diyl)] (PBT4T‐2OD), where the fluorine atoms in the benzothiadiazole moieties of PffBT4T‐2OD are replaced with hydrogen atoms; and (iii) poly[(2,2′‐bithiophene)‐alt‐(4,7‐bis((2‐decyltetradecyl)thiophen‐2‐yl)‐5,6‐difluoro‐2‐propyl‐2H‐benzo[d][1,2,3]triazole)] (PT2‐FTAZ), where the sulfur atoms in the benzothiadiazole moieties of PffBT4T‐2OD are replaced with nitrogen atoms carrying a linear C3H7 side‐chain; these polymers are mixed with the phenyl‐C71‐butyric acid methyl ester (PC71BM) acceptor. This study also discusses the nature of the charge‐transfer electronic states appearing at the donor–acceptor interfaces, the electronic couplings relevant for the charge‐recombination process, and the electron‐transfer features between neighboring PC71BM molecules.  相似文献   
7.
Cr2O3 nanoparticles have been prepared for precipitation technique at reaction temperature 50 °C. The prepared samples were annealed different temperatures at 500,700 and 1000 °C. Synthesized powders were characterized as X-ray diffraction, optical, transmission electron microscope, SEM with EDAX, humidity sensor, FTIR. The annealing temperature has been found to be playing a crucial role in the controlling particle size. XRD study shows the rhombohedral crystal structure of highly preferential orientation along (1 0 4) direction. FTIR reveals that the presence Cr–O bonds in the structure. The TEM images show that the size of NPs of Cr2O3 varied from 26 to 60 nm with average crystalline size 43 nm. UV–visible spectrum shows the absorption band of Cr2O3 nanoparticles at 400 nm. The humidity sensor of the Cr2O3 nanoparticles was studied by two temperature method. 1000 °C annealed Cr2O3 nanoparticles show better sensing properties and exhibits good linearity in response than 500 °C. SEM images show the clusters and agglomeration of nanoparticles. EDAX spectrum confirms the presence of Cr2O3 nanoparticles. Each samples have been characterized as sensing materials to determine relative humidity in the range of 20–90%. The humidity sensing property increased with increasing of annealing temperature and the resistance was decreased.  相似文献   
8.
Polyaniline is a widely studied conducting polymer and is a useful material in its bulk and thin film form for many applications, because of its excellent optical and electrical properties. Pristine and iodine doped polyaniline thin films were prepared by a.c. and rf plasma polymerization techniques separately for the comparison of their optical and electrical properties. Doping of iodine was effectedin situ. The structural properties of these films were evaluated by FTIR spectroscopy and the optical band gap was estimated from UV-vis-NIR measurements. Comparative studies on the structural, optical and electrical properties of a.c. and rf polymerization are presented here. It has been found that the optical band gap of the polyaniline thin films prepared by rf and a.c. plasma polymerization techniques differ considerably and the band gap is further reduced byin situ doping of iodine. The electrical conductivity measurements on these films show a higher value of electrical conductivity in the case of rf plasma polymerized thin films when compared to the a.c. plasma polymerized films. Also, it is found that the iodine doping enhanced conductivity of the polymer thin films considerably. The results are compared and correlated and have been explained with respect to the different structures adopted under these two preparation techniques.  相似文献   
9.
Infrared focal plane arrays (IRFPAs) are rapidly increasing in size. It is shown here that for large FPAs a considerable shift in the operating point occurs, which, if not reduced, introduces unacceptably large nonuniformity in the array response. This shift results because of the variable voltage drop across the HgCdTe active layer, due to its finite distributed resistance. A new analytical two-dimensional (2-D) model to estimate the operating point shift of individual detectors of long wavelength infrared (LWIR) HgCdTe focal plane array (FPA) is presented. Avoiding this operating point shift requires an optimized grid pattern  相似文献   
10.
Although tumor-antigen-based therapeutic cancer vaccines are a potential cancer immunotherapy strategy, recent clinical trials show low efficacy for multiple reasons. One method that has been recently investigated to improve the efficacy of therapeutic cancer vaccines is the development of implantable vaccines for sustained delivery of antigens and CD8 T cell activation. Here, we optimized the composition for an implantable vaccine scaffold composed of alginate, polyvinyl alcohol, and poly(methyl vinyl ether- alt-maleic anhydride) loaded with tumor antigens. Considering the adjuvant property of aluminum compounds, aluminum ion was used to crosslink alginate in the scaffold. The scaffold showed an effective antigen incorporation efficiency of 90.34 ± 0.55% using ovalbumin as the model antigen and 89.67 ± 2.8% using B16-F10 cell lysate. SEM analysis of the scaffold showed pore size ranging from 5 to 10 μm. Cell viability analysis using mouse RAW 264.7 macrophages proved the cytocompatibility of the scaffold. In vitro antigen release studies using ovalbumin showed 8.42% release for a period of 14 days. In vivo antitumor analysis carried out in subcutaneous mouse B16-F10 melanoma model demonstrated that the scaffold vaccine reduced the rate of tumor growth and improved survival in tested animals. The median survival time increased from 29 days in untreated animals to 58 days in scaffold vaccine-implanted animals.  相似文献   
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