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31.
ABSTRACT

Magnesium layered hydroxide (MLH) intercalated with anionic 3-(4-methoxyphenyl)propionic acid (MPP) was synthesised by a direct reaction method using magnesium oxide and MPP as precursors. A further coating of chitosan was applied on the external surface of MLH–MPP nanocomposite to form a new material, named MLH–MPP/chitosan nanocomposite. The XRD pattern showed an intense and sharp peak at basal spacing 18.9 Å, proving that MPP anions were successfully intercalated into the interlayer gallery of MLH in a monolayer arrangement. The XRD pattern of the MLH–MPP/chitosan nanocomposite shows similar peaks with the MLH–MPP nanocomposite. The result was also supported by FTIR spectra and elemental analysis. TGA/DTG spectra showed that the thermal stabilities of the guest anion in the both nanocomposites were markedly enhanced. A controlled-release study of the MPP ion from the MLH–MPP/chitosan nanocomposite showed a slower release compared to MLH–MPP nanocomposite with an initial rapid release and slow release thereafter. Meanwhile, the release behaviours of MPP ions from both nanocomposites were governed by pseudo-second order kinetics. This result highlights the potential of the nanocomposite as an encapsulated material for the controlled-release formulation of MPP anions.  相似文献   
32.
In this study, nanocrystalline magnesium zinc ferrite nanoparticles were successfully prepared by a simple sol–gel method using copper nitrate and ferric nitrate as raw materials. The calcined samples were characterised by differential thermal analysis/thermogravimetric analysis, Fourier transform infrared spectroscopy and X‐ray diffraction. Transmission electron microscopy revealed that the average particle size of the calcined sample was in a range of 17–41 nm with an average of 29 nm and has spherical size. A cytotoxicity test was performed on human breast cancer cells (MDA MB‐231) and (MCF‐7) at various concentrations starting from (0 µg/ml) to (800 µg/ml). The sample possessed a mild toxic effect toward MDA MB‐231 and MCF‐7 after being examined with MTT (3‐[4, 5‐dimethylthiazol‐2‐yl]‐2, 5 diphenyltetrazolium bromide) assay for up to 72 h of incubation. Higher reduction of cells viability was observed as the concentration of sample was increased in MDA MB‐231 cell line than in MCF‐7. Therefore, further cytotoxicity tests were performed on MDA MB‐231 cell line.Inspec keywords: sol‐gel processing, nanoparticles, nanofabrication, magnesium compounds, zinc compounds, toxicology, biological organs, cancer, cellular biophysics, nanomedicine, calcination, differential thermal analysis, Fourier transform infrared spectra, X‐ray diffraction, transmission electron microscopy, particle size, organic compoundsOther keywords: sol‐gel method, cytotoxic effects, breast cancer cell line, MDA MB‐231 in vitro, nanocrystalline magnesium zinc ferrite nanoparticles, copper nitrate, ferric nitrate, raw materials, calcined samples, differential thermal analysis, thermogravimetric analysis, Fourier transform infrared spectroscopy, X‐ray diffraction, transmission electron microscopy, average particle size, cytotoxicity testing, human breast cancer cells, mild toxic effect, 3‐[4,5‐dimethylthiazol‐2‐yl]‐2,5 diphenyltetrazolium bromide) assay, cell viability, MCF‐7, MDA MB‐231 cell line, size 17 nm to 41 nm  相似文献   
33.
An investigation is reported of the 75 at% nickel section of the Ni-Cr-Al-Ru system at 1523 and 1273 K. Constitutional data obtained by electron probe microanalysis, X-ray diffraction and microscopical examination are presented as partial isothermal sections. At 1523 K, the major part of the section consists of phase, while the aluminium-rich region contains a and+ region; the extent of the solid solution of chromium and ruthenium in totals ~ 4 at%. The ruthenium-rich corner of the section shows a two-phase region consisting of + ruthenium-rich solid solution. At 1273 K the,+ and + ruthenium regions increase in extent. The/ mismatch values in the equilibrated alloys studied lie in the range ~ –0.08 to –0.39%. Constitutional features of as-cast alloys are also reported.  相似文献   
34.
An electronic nose was successfully used to detect and discriminate lard from other types of animal body fats and samples containing lard. The results are presented in the form of VaporPrint™, the image of the polar plot of the odor amplitudes from the surface acoustic wave (SAW) detector frequency. In the VaporPrint™, the radial angles representing the sensor provides individual fingerprints of the aroma of different animal body fats. Principal component analysis (PCA) was used to interpret the data and it provided a good grouping of samples, with 61% of the variation accounted for by PC 1 and 29% accounted for by PC 2. All of the lard-containing samples formed a separate group from the samples that were free from lard. This method can be developed into a rapid method for detecting the presence of lard in food samples for Halal authentication.  相似文献   
35.
BACKGROUND: Much attention has been given to applying ionic liquids (ILs) as an alternative pretreatment method for lignocellulosic biomass. This study aims to select the most suitable type of IL for pretreating sugarcane bagasse (SCB). The potential of ILs for pretreatment was evaluated and compared with conventional pretreatment media, acids and alkalis. The performance of the pretreatment media was evaluated based on the amount of reducing sugar produced from enzymatic saccharification, the energy requirement, and changes in the chemical structure and crystallinity index of the pretreated bagasse. RESULTS: 1‐ethyl‐3‐methylimidazolium acetate [EMIM]oAc was selected as the most suitable IL for SCB pretreatment. The optimum yields of reducing sugar obtained from [EMIM]oAc‐, alkali‐, and acid‐pretreated SCB were 69.5%, 92.8% and 41.3%, respectively. Although a lower yield of reducing sugar was obtained, [EMIM]oAc pretreatment required the least energy to pretreat 1 kg of SCB. Moreover, the percentage of SCB loss during [EMIM]oAc pretreatment was the lowest. [EMIM]oAc‐pretreated SCB also had the lowest crystallinity index (CI) with the most amorphous structure. CONCLUSION: [EMIM]oAc appears to be another option for pretreating SCB, and other issues such as the recyclability of [EMIM]oAc is worth investigating. Copyright © 2011 Society of Chemical Industry  相似文献   
36.
37.
The mutual separation of a mixture of cetyltrimethyl ammonium chloride (CTAC), methyl trioctyl ammonium bromide (MTOB), dodecyltrimethyl ammonium chloride (DTAC), benzyltrimethyl ammonium chloride (BTAC) and tetrabutyl ammonium bromide (TBAB), was achieved on silica high performance thin layer chromatographic plates using dimethyl sulfoxide with aqueous sodium-l-tartrate dibasic dihydrate as the solvent system. The effect of concentration of sodium-l-tartrate dibasic dihydrate on the mobility of all the five quaternaries was examined. The limit of detection of CTAC, MTOB, DTAC, BTAC and TBAB was estimated as 0.6, 0.6, 0.3, 0.6 and 0.3 μg/zone, respectively. The method developed was utilized to identify these surfactants in different spiked water samples after their preliminary separation.  相似文献   
38.
In order to classify unknown gelatin into their species of origin, a simple and rapid method for the qualitative determination was developed using Fourier transform infrared (FTIR) in combination with attenuated total reflectance (ATR) and discriminant analysis. The spectra were analysed using a chemometric method, principal component analysis (PCA), to classify and characterise gelatin compounds using regions of the FTIR spectra in the range of 3290–3280 cm?1 and 1660–1200 cm?1 as calibration models. Results from PCA, which were subsequently represented by the Cooman’s plot showed a clear distinction between gelatin samples of bovine and porcine origins. This qualitative approach, besides providing a rapid determination of the source of gelatin, may also be established based on a second derivative study of the FTIR spectrum to alleviate any doubt of the gelatin source for applications in the food and pharmaceutical industries.  相似文献   
39.
Medium density fiberboard (MDF) is one of the widely used wood-based panels to manufacture building components such as furniture units for interior applications. Although MDF is an excellent product it is prone to fire hazard which should be enhanced using flame retardants during its manufacture. Properties of the flame retardant urea formaldehyde (UF) MDF made using a dry process from rubberwood fibers were investigated. Flame retardant chemicals that were evaluated include sodium aluminate, zinc borate and aluminum trihydrate, which were incorporated with rubberwood fibers to manufacture experimental MDF. Four concentration levels, 10%, 15%, 20% and 30% of fire retardants and 15% urea formaldehyde resin based on oven dry fiber weight were used to manufacture experimental panels. Physical and mechanical properties including thickness swelling, water absorption, bending characteristics, and internal bond strength of the samples were determined. Flame retardant properties of the panels were also investigated using a Cabinet Method along with char index, weight loss and size of ellipse area. Finally, thermogravimetry method was employed to analyze thermal properties of the MDF panels. The results showed that thickness swell and water absorption decreased as the flame retardant increased. The MOR was not affected by the flame retardant treatment for boards bonded with urea formaldehyde resin. The internal bond strength showed a small reduction compared with the controls as the flame retardant chemicals increased but not for boards treated with 5% aluminum trihydrate. When the concentration of flame retardant chemicals increased to 30%, the internal bond generally decreased. Char index, area of ellipse and weight loss reduced as the percentage of flame retardant increased. Sodium aluminate showed the best performance in reducing thermal degradation followed by aluminum trihydrate and zinc borate. Aluminum trihydrate cured closely resemble that of the control during the gelation test.  相似文献   
40.
Colloidal gas aphrons (CGAs), generated from dilute solutions of four surfactants, were used to clarify palm oil mill effluent (POME), suspensions of microalgae and suspensions of three inorganic minerals. In POME and the algal suspensions, each CGA was most effective at a pH value close to the pK value of the surfactant concerned. This effect was not tested in the inorganic suspensions. The efficiency of air utilization was directly related to the concentration of solids in the suspensions, the size, density and nature of the solids having secondary effects. Comparison with data in the literature led to a general correlation embracing a variety of suspensions and flotation systems. Shedding of collected material from the foam layer was also a direct function of solids concentration. CGAs offer advantages over other systems of air-assisted flotation in relation to the requirements for equipment and to the management of process operations.  相似文献   
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