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1.
Polyacrylonitrile (PAN) based polymer electrolyte membranes complexed with Ammonium hexafluorophosphate (NH4PF6) with different molar concentration are prepared by solution casting method. Increase in the amorphous nature by the addition of Ammonium salt and the formation of polymer-salt complex are confirmed by X ray diffraction studies and infrared spectroscopy respectively. The glass transition temperature is measured for all membranes and it showed a lowest value for the PAN complexed with 20 mol% of NH4PF6. Electrical properties are studied by AC impedance spectroscopy. An ionic conductivity of the order of 10?3 Scm?1 is obtained for the 80 PAN / 20 NH4PF6 polymer electrolyte. Conductivity, dielectric and modulus spectra from the impedance data are analysed to understand the ionic transport mechanism. Transference number measurement is done to study the ionic contribution to the charge transport. A proton battery with the configuration, Zn+ ZnSO4. 7H2O /80 PAN / 20 NH4PF6 / PbO2 +V2O5 has been constructed and its discharge characteristics are studied.  相似文献   
2.
In this present study, the compression ignition engine was designed to run on CIME (Calophyllum inophyllum methyl ester) biodiesel with nanoparticles. The TiO2 nanoparticle is added to the biodiesel in the form of nanofluid at concentration levels of 100?ppm whereas ethanox is added at levels of 100, 200 and 500?ppm. The nanoparticle and the ethanox are dispersed by the ultrasonication process. The addition of nanofluid reduces the particulate emission like nitrogen oxide (NOx) at 100% load. The efficiency is better and emission is reduced owing to the influence of explosion of water molecules present in the biodiesel. We found ethanox to be a superlative nanofluid to reduce the emission of toxic gas at appreciable levels. We have witnessed a 20% reduction in emission of NOx and 10% reduction of other particulate emission. In addition, the exit geometry of exhaust is modified from a circular shape to an elliptical one and the consequence of the geometry is calculated.  相似文献   
3.
In this present study, a hybrid Chi‐Fe3 O4 was prepared, characterised and evaluated for its antibacterial and antibiofilm potential against Staphylococcus aureus and Staphylococcus marcescens bacterial pathogens. Intense peak around 260 nm in the ultraviolet–visible spectrum specify the formation of magnetite nanoparticles. Spherical‐shaped particles with less agglomeration and particle size distribution of 3.78–46.40 nm were observed using transmission electron microscopy analysis and strong interaction of chitosan with the surface of magnetite nanoparticles was studied using field emission scanning microscopy (FESEM). X‐ray diffraction analysis exhibited the polycrystalline and spinel structure configuration of the nanocomposite. Presence of Fe and O, C and Cl elements were confirmed using energy dispersive X‐ray microanalysis. Fourier transform infrared spectroscopic analysis showed the reduction and formation of Chi‐Fe3 O4 nanocomposite. The antibacterial activity by deformation of the bacterial cell walls on treatment with Chi‐Fe3 O4 nanocomposite and its interaction was visualised using FESEM and the antibiofilm activity was determined using antibiofilm assay. In conclusion, this present study shows the green synthesis of Chi‐Fe3 O4 nanocomposite and evaluation of its antibacterial and antibiofilm potential, proving its significance in medical and biological applicationsInspec keywords: visible spectra, particle size, magnetic particles, nanocomposites, nanoparticles, X‐ray diffraction, nanofabrication, transmission electron microscopy, X‐ray chemical analysis, nanomagnetics, microorganisms, antibacterial activity, iron compounds, ultraviolet spectra, biomedical materials, field emission scanning electron microscopy, Fourier transform infrared spectra, filled polymers, crystal growth from solution, polymer structureOther keywords: potential antibacterial material, antibiofilm potential, magnetite nanoparticles, solvothermal‐assisted green synthesis, hybrid Chi‐Fe3 O4 nanocomposites, staphylococcus aureus, staphylococcus marcescens, bacterial pathogens, ultraviolet–visible spectrum, spherical‐shaped particles, particle size, transmission electron microscopy, FESEM, field emission scanning electron microscopy, X‐ray diffraction, spinel structure, polycrystalline structure, energy dispersive X‐ray microanalysis, Fourier transform infrared spectroscopic analysis, deformation, bacterial cell walls, Fe3 O4   相似文献   
4.
Nanocrystalline ceria has been synthesized by a non-hydrolytic method using organic solvent and precipitant. The effect of the source compound on final nanocrystalline powder was investigated. The cerium nitrate hexahydrate subjected to different vacuum/thermal treatments to get cerium source compound having different extent of water of crystallization. The nanoceria, synthesized from these compounds was characterized by TGA-MS, XRD, HR-TEM and AFM.  相似文献   
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6.
A dendritic-benzimidazole (D-BI) has been prepared using polyphosphoric acid (PPA) as a condensing medium with diaminobenzidine (DAB), 1,3,5-benzene tricarboxylic acid, and isophthalic acid as monomers. The structure of D-BI was ascertained by elemental analysis, FTIR, 1H NMR, and solid-state 13C-NMR. The D-BI was incorporated into polysulphone (PSf) by blending with polyvinylpyrrolidone (PVP K-30) as a macromolecular additive. The membranes were cast by phase inversion technique. The physical properties such as surface morphology and the chemical properties such as contact angle and the performance attributes, such as NOM rejection, salt rejection, and pure water flux were studied. It is imperative that the infusibility of rigid polymeric backbone is overcome by the introduction of polar moieties with no compromise on thermal stability. The membranes displayed substantial increase in thermal stability with D-BI content. The marginal increase in flux has been attributed to the branching and steric effect of D-BI. This is because the introduction of polar group efficiently affords to stabilize the adjacent aromatic rings. The salt rejection shows the order of MgSO4 ≈ Na2SO4 > MgCl2 > NaCl, which follows that the divalent ions are rejected more than monovalent ions. The antifouling behaviour was also significant as the irreversible fouling (RIr 9%), which was found to be minimal for D-BI-incorporated membrane. The blended membranes exhibited good hydrophilicity, antifouling, and fairly good rejection of salts.  相似文献   
7.
Wireless Personal Communications - Resource allocation assigns subcarriers and power at the Base Station (BS) to different users, and is an important aspect in multiuser OFDMA downlink (DL)...  相似文献   
8.
The present research is focused on the development of ecofriendly biopolymer blend based nanocomposites to enhance the effect of cytotoxic activity. Novel eco-friendly synthesis of pure Chitosan–Agar blend and Chitosan–Agar/ZnO nanocomposites was successfully synthesized by in-situ chemical synthesis method. The influence of Chitosan–Agar (1:1 wt/wt%) concentrations (0.1, 0.5, 1 and 3 g) was studied. The presence of ZnO nanoparticles in Chitosan–Agar polymer matrix was confirmed by UV, FTIR, XRD, FESEM, EDAX and TEM. The crystallite size of the nanocomposites in the range of 12–17 nm is observed from XRD analysis. PL and UV reveal that Nanocomposites shows an blue shift by increase in the blend concentrations. TEM analysis shows that 0.1 and 3 g of Chitosan–Agar/ZnO Nanocomposites are in spindle and spherical shape with polycrystalline nature. The prepared Nanocomposites shows the respectable Antibacterial activity against Gram-positive (Staphylococcus aureus and Bacillus subtilis) and Gram-negative (Pseudomonas aureginosa and Klebsilla pneumonia) bacteria. The potential toxicity of Chitosan–Agar/ZnO nanocomposites was studied for normal (L929) and breast cancer cell line (MB231). The result of this investigation shows that the Chitosan–Agar/ZnO nanocomposites deliver a dose dependent toxicity in normal and cancer cell line.  相似文献   
9.
ABSTRACT

Nanostructured Mg2Ni intermetallic compounds were synthesized by high-energy ball milling. Effect of milling time on structure and surface morphology of milled powders were studied using x-ray diffraction and scanning electron microscopy. Crystallite size and degree of crystallinity were confirmed by using transmission electron microscopy and selected area electron diffraction analysis. The particle size of 20 h milled electrode material is 230 nm and it reduced to 40 nm when the milling time is increased to 30 h. Further increase in the milling time reduces the particles size drastically and starts agglomerating. In order to understand the effect of milling time on reaction rates, differential thermal analysis was performed. Activation energy of the milled powders was calculated using Kissinger analysis. 30 h milled powder exhibits lower activation energy than others. Cyclic voltammetry, electrochemical impedance spectroscopy, and charge–discharge studies were done on the prepared electrode materials. 30 h milled electrode material delivers maximum discharge capacity with a superior capacity retention after 20 cycles at 20 mAg?1.  相似文献   
10.
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