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41.
FeO-doped TiO2 nanoparticle photocatalysts were immobilized onto the surface of fibrous activated carbon (ACF) via a sol-gel process. As an adsorbent and photocatalyst, FeO-TiO2 on immobilized ACFs (FeO-TiO2/ACF) greatly improved the photocatalysis rate of hydrogen production as compared with pure TiO2 and ACF-TiO2 under UV irradiation and visible light. The addition of ACFs surface significantly reduced the photogenerated pairs of electrons-hole recombination, thereby promoting the photocatalysis action of doped photo-metal oxides of FeO-TiO2. Co-doping of FeO onto the lattice of the TiO2 approach can improve the absorption activity of visible light through photo-metal oxide of TiO2 and further enhance hydrogen production under visible light. The photocatalytic fabrics (FeO-TiO2/ACF) were effortlessly split out from the experimental solution for re-utilization and exhibited high stability even after five complete regeneration cycles.  相似文献   
42.
This work proposes a transient heat transfer model to predict the thermal behaviour of wood in a heated bed of sand fluidized with nitrogen. The 2-D model in cylindrical coordinates considers wood anisotropy, variable fuel properties, fuel particle shrinkage, and heat generation due to drying and devolatilization. The influence of initial fuel moisture content, thermal diffusivity, particle geometry, shrinkage, external heat transfer coefficient, chemical reaction kinetics and heats of reaction on temperature rise is presented. The cylindrical wood particles chosen for the study have length (l) = 20 mm, diameter (d) = 4 mm and l = 50 mm and d = 10 mm, both having an aspect ratio (l/d) of 5. The bed temperature is 1123 K. The model prediction is validated using measurements obtained from literature. The temperature rise in the wood particle is found to be sensitive to changes in the moisture content and thermal diffusivity and heat of reaction (in larger particles) while it is less sensitive to the external heat transfer coefficient and chemical kinetics. Also shrinkage is found to have a compensating effect and it does not have any significant influence on the temperature rise. Beyond an aspect ratio of three, the wood particle behaves as a 1-D cylinder.  相似文献   
43.
The interaction of the nucleocapsid NCp7 of the human immunodeficiency virus type 1 (HIV-1) Gag polyprotein with the RNA packaging signal Psi ensures specific encapsidation of the dimeric full length viral genome into nascent virus particles. Being an essential step in the HIV-1 replication cycle, specific genome encapsidation represents a promising target for therapeutic intervention. We previously selected peptides binding to HIV-1 Psi-RNA or stem loops (SL) thereof by phage display. Herein, we describe synthesis of peptide variants of the consensus HWWPWW motif on membrane supports to optimize Psi-RNA binding. The optimized peptide, psi-pepB, was characterized in detail with respect to its conformation and binding properties for the SL3 of the Psi packaging signal by NMR and tryptophan fluorescence quenching. Functional analysis revealed that psi-pepB caused a strong reduction of virus release by infected cells as monitored by reduced transduction efficiencies, capsid p24 antigen levels, and electron microscopy. Thus, this peptide shows antiviral activity and could serve as a lead compound to develop new drugs targeting HIV-1.  相似文献   
44.
Well-defined poly(n-docosyl acrylate) (PDA) with narrow molecular weight distribution has been synthesized by atom transfer radical polymerization (ATRP) and reverse ATRP of n-docosyl acrylate (DA) at 80 °C in N,N-dimethylformamide using the carbon tetrabromide/FeCl3/2,2′-bipyridine (bpy) initiation system in the presence of 2,2′-azobisisobutyronitrile (AIBN) and benzoyl peroxide (BPO) as the source of reducing agent. The rates of polymerization for both the systems exhibit first-order kinetics with respect to the monomer, however, peroxide-initiated system shows slow rate of polymerization as compared to the azo-system. The effect of various reaction parameters on number average molecular weight (M n ) and molecular weight distribution (M w/M n ) have been investigated. The resulting PDA that obtained in presence of AIBN and BPO systems has been compared for both the conventional and reverse ATRP. The reverse ATRP initiated by peroxides behaves differently than that of the azo initiators. In reverse ATRP with BPO, the rate of polymerization (R p) has been significantly increased with the increase of BPO resulting higher M n and broader M w/M n . The reverse ATRP of DA did not exhibit living characteristics with BPO system. PDA has been characterized by GPC, FTIR, and NMR spectroscopy.  相似文献   
45.
A new, simple, and rapid high-performance thin-layer chromatographic method with a derivatization procedure was developed and validated for quantitative determination of tacrolimus. Tacrolimus was chromatographed on silica gel 60 F254 TLC plate using toluene–acetonitrile–glacial acetic acid (6:4:0.1, by volume) as mobile phase. Tacrolimus was visualized using a derivatization reagent containing anisaldehyde–sulfuric acid in absolute alcohol and quantified by densitometric analysis in the reflectance mode at 675 nm. The method was found to give compact spots for the drug (Rf?=?0.40?±?0.03). The linear regression analysis data for the calibration plots showed good linear relationship with r2?=?.9989 in the concentration range 100–800 ng/spot. The method was validated for precision, recovery, repeatability, and robustness as per the International Conference on Harmonization guidelines. The minimum detectable amount was found to be 28.90 ng, whereas the limit of quantitation was found to be 97.04 ng. Statistical analysis of the data showed that the method is precise, accurate, reproducible, and selective for the analysis of tacrolimus. The method was successfully employed for the estimation of equilibrium solubility and quantification of tacrolimus as a bulk drug and in commercially available capsules and in-house developed self-microemulsifying formulations.  相似文献   
46.
Bandpass frequency-selective surfaces (FSSs) controlled by varactors and representing biperiodic lattices formed from slotted squares in a thin metallic screen are considered. Main factors affecting the FSS tuning range with different circuits for connection of control varactors are experimentally evaluated. Experimental results obtained by the waveguide method of measuring the transmission coefficient through samples of both individual FSS elements loaded with varactors of various types and lattices consisting of these elements at microwave frequencies are presented. Based on the measured data, attainable values of the relative tuning of the FSS resonance frequency are evaluated: f max/f min = 1.4 for control circuits with two MA46N120 low-capacitance varactors in each FSS element and f max/f min = 1.5 for control circuits with one VV857 medium-capacitance varactor.  相似文献   
47.
The present state of the development and production of Russian and foreign radio-measuring instruments in the frequency range up to 178.4 GHz (and higher) and the proposed glossary of the new generation of Russian instruments are considered.  相似文献   
48.
The temporal behavior of light collection in the 1.5-m3-volume mirror-reflecting counter filled with a highly transmitting liquid scintillator has been investigated. Using the Monte Carlo method and assuming that the luminescence decay time of the liquid scintillator is zero (τLS = 0), it has been ascertained that, in the case of a short flash in a counter, the exponential phase of light collection is characterized by time τcol = 15.0 ± 1.7 ns, which is does not depend on scattering of light in the medium. The measured exponent index τact = 37 ± 3 ns of an actual pulse due to a muon is determined both by light collection time τcol ≈ 15 ns and luminescence decay time τLS ≈ 20 ns of the scintillator in the large-volume counter.  相似文献   
49.
50.
In the present communication we report on the optimization of persulfate/ascorbic acid initiated synthesis of chitosan-graft-poly(acrylamide) (Ch-g-PAM) and its application in the removal of azo dyes. The optimum yield of the copolymer was obtained using 16 × 10−2 M acrylamide, 3.0 × 10−2 M ascorbic acid, 2.4 × 10−3 M K2S2O8 and 0.1 g chitosan in 25 mL of 5% aqueous formic acid at 45 ± 0.2 °C. Ch-g-PAM remained water insoluble even under highly acidic conditions and could efficiently remove Remazol violet and Procion yellow dyes from the aqueous solutions over a pH range of 3–8 in contrast to chitosan (Ch) which showed pH dependent adsorption. The adsorption data of the Ch-g-PAM and Ch for both the dyes were modeled by Langmuir and Freundlich isotherms where the data fitted better to Langmuir isotherms. To understand the adsorption behavior of Ch-g-PAM, adsorption of Remazol violet on to the copolymer was optimized and the kinetic and thermodynamic studies were carried out taking Ch as reference. Both Ch-g-PAM and Ch followed pseudo-second-order adsorption kinetics. The thermodynamic study revealed a positive heat of adsorption (ΔH°), a positive ΔS° and a negative ΔG°, indicating spontaneous and endothermic nature of the adsorption of RV dye on to the Ch-g-PAM. The Ch-g-PAM was found to be very efficient in removing color from real industrial wastewater as well, though the interfering ions present in the wastewater slightly hindered its adsorption capacity. The data from regeneration efficiencies for ten cycles evidenced the high reusability of the copolymer in the treatment of waste water laden with even high concentrations of dye.  相似文献   
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