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101.
102.
A Roman dominating function on a graph G = (V, E) is a function f : V ? {0, 1, 2}f : V \rightarrow \{0, 1, 2\} satisfying the condition that every vertex v for which f(v) = 0 is adjacent to at least one vertex u for which f(u) = 2. The weight of a Roman dominating function is the value w(f) = ?v ? V f(v)w(f) = \sum_{v\in V} f(v). The Roman domination number of a graph G, denoted by gR(G)_{\gamma R}(G), equals the minimum weight of a Roman dominating function on G. The Roman domination subdivision number sdgR(G)sd_{\gamma R}(G) is the minimum number of edges that must be subdivided (each edge in G can be subdivided at most once) in order to increase the Roman domination number. In this paper, first we establish upper
bounds on the Roman domination subdivision number for arbitrary graphs in terms of vertex degree. Then we present several
different conditions on G which are sufficient to imply that $1 \leq sd_{\gamma R}(G)
\leq 3$1 \leq sd_{\gamma R}(G)
\leq 3. Finally, we show that the Roman domination subdivision number of a graph can be arbitrarily large. 相似文献
103.
The increasing demand for low-cost and high performance coatings has promoted the development of chip epoxy-based coatings using inert fillers. Attention has been paid here on employing mixtures of DGEBA with barium carbonate as novel ceramic-based filler to produce a coating using 1,8-naphthalene diamine (1,8-NDA) as the crosslinking agent. A substantial increase in the Tg, from 85 to 100 °C, is observed for the optimum composition. The 1,8-NDA-cure of the epoxy composites showed an autocatalytic mechanism. At a specific conversion range the cure reaction of the composites will be controlled by a diffusion-control cure reaction rather than by Kamal autocatalytic model. Model-free isoconversional method is utilized to construct apparent activation energy dependence on conversion plot. The effect of diffusion control is described by an approach proposed by Chern and Poehlein. Greater diffusion control is observed as the cure temperature decreased. 相似文献
104.
Mohammad Ghalambaz Seyed Abdollah Mansouri Mehryan Kasra Ayoubi Ayoubloo Ahmad Hajjar Mohamad El Kadri Obai Younis Mohsen Saffari Pour Christopher Hulme-Smith 《Molecules (Basel, Switzerland)》2021,26(5)
Thermal energy storage units conventionally have the drawback of slow charging response. Thus, heat transfer enhancement techniques are required to reduce charging time. Using nanoadditives is a promising approach to enhance the heat transfer and energy storage response time of materials that store heat by undergoing a reversible phase change, so-called phase change materials. In the present study, a combination of such materials enhanced with the addition of nanometer-scale graphene oxide particles (called nano-enhanced phase change materials) and a layer of a copper foam is proposed to improve the thermal performance of a shell-and-tube latent heat thermal energy storage (LHTES) unit filled with capric acid. Both graphene oxide and copper nanoparticles were tested as the nanometer-scale additives. A geometrically nonuniform layer of copper foam was placed over the hot tube inside the unit. The metal foam layer can improve heat transfer with an increase of the composite thermal conductivity. However, it suppressed the natural convection flows and could reduce heat transfer in the molten regions. Thus, a metal foam layer with a nonuniform shape can maximize thermal conductivity in conduction-dominant regions and minimize its adverse impacts on natural convection flows. The heat transfer was modeled using partial differential equations for conservations of momentum and heat. The finite element method was used to solve the partial differential equations. A backward differential formula was used to control the accuracy and convergence of the solution automatically. Mesh adaptation was applied to increase the mesh resolution at the interface between phases and improve the quality and stability of the solution. The impact of the eccentricity and porosity of the metal foam layer and the volume fraction of nanoparticles on the energy storage and the thermal performance of the LHTES unit was addressed. The layer of the metal foam notably improves the response time of the LHTES unit, and a 10% eccentricity of the porous layer toward the bottom improved the response time of the LHTES unit by 50%. The presence of nanoadditives could reduce the response time (melting time) of the LHTES unit by 12%, and copper nanoparticles were slightly better than graphene oxide particles in terms of heat transfer enhancement. The design parameters of the eccentricity, porosity, and volume fraction of nanoparticles had minimal impact on the thermal energy storage capacity of the LHTES unit, while their impact on the melting time (response time) was significant. Thus, a combination of the enhancement method could practically reduce the thermal charging time of an LHTES unit without a significant increase in its size. 相似文献
105.
Abdollah Salimi Mohadeseh Izadi Rahman Hallaj Saied Soltanian Hassan Hadadzadeh 《Journal of Solid State Electrochemistry》2009,13(3):485-496
A simple procedure was developed to prepare a glassy carbon electrode modified with carbon nanotubes and Ruthenium (III) complexes.
First, 25 μl of dimethyl sulfoxide–carbon nanotubes solutions (0.4 mg/ml) was cast on the surface of the glassy carbon electrode
and dried in air to form a carbon nanotube film at the electrode surface. Then, the glassy carbon/carbon nanotube-modified
electrode was immersed into a Ruthenium (III) complex solution (direct deposition) for a short period of time (10–20 s for
multiwalled carbon nanotubes and 20–40 s for single-walled carbon nanotubes). The cyclic voltammograms of the modified electrode
in aqueous solution shows a pair of well-defined, stable, and nearly reversible redox couple, Ru(III)/Ru(II), with surface-confined
characteristics. The attractive mechanical and electrical characteristics of carbon nanostructures and unique properties and
reactivity of Ru complexes are combined. The transfer coefficient (α), heterogeneous electron transfer rate constants (k
s), and surface concentrations (Γ) for the glassy carbon/single-walled carbon nanotubes/Ru(III) complex-, glassy carbon/multiwalled carbon nanotubes/Ru(III)
complex-, and glassy carbon/Ru(III) complex-modified electrodes were calculated using the cyclic voltammetry technique. The
modified electrodes showed excellent catalytic activity, fast response time, and high sensitivity toward the reduction of
nicotinamide adenine dinucleotide in phosphate buffer solutions at a pH range of 4–8. The catalytic cathodic current depends
on the nicotinamide adenine dinucleotide concentration. In the presence of alcohol dehydrogenase, the modified electrode exhibited
a response to addition of acetaldehyde. Therefore, the main product of nicotinamide adenine dinucleotide electroreduction
at the Ru(III) complex/carbon nanotube-modified electrode was the enzymatically active NADH. The purposed sensor can be used
for acetaldehyde determination. 相似文献
106.
Abdollah Noorbakhsh Mohmmad Khakpoor Mohammad Rafieniya Ensiyeh Sharifi Mohammad Mehrasa 《Electroanalysis》2017,29(4):1113-1123
The present study describes a novel and very sensitive electrochemical assay for determination of hydrogen peroxide (H2O2) based on synergistic effects of reduced graphene oxide‐ magnetic iron oxide nanocomposite (rGO‐Fe3O4) and celestine blue (CB) for electrochemical reduction of H2O2. rGO‐Fe3O4 nanocomposite was synthesized and characterized by Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), X‐ray diffraction (XRD), electrochemical impedance spectroscopy and cyclic voltammetry. Chitosan (Chit) was used for immobilization of amino‐terminated single‐stranded DNA (ss‐DNA) molecules via a glutaraldehyde (GA) to the surface of rGO‐Fe3O4. The MTT (3‐(4,5‐Dim ethylt hiazol‐2‐yl)‐2,5‐diphenylt etrazolium bromide) results confirmed the biocompatibility of nanocomposite. Experimental parameters affecting the ss‐DNA molecules immobilization were optimized. Finally, by accumulation of the CB on the surface of the rGO‐Fe3O4‐Chit/ssDNA, very sensitive amperometric H2O2 sensor was fabricated. The electrocatalytic activity of the rGO‐Fe3O4‐Chit/DNA‐CB electrode toward H2O2 reduction was found to be very efficient, yielding very low detection limit (DL) of 42 nM and a sensitivity of 8.51 μA/μM. Result shows that complex matrices of the human serum samples did not interfere with the fabricated sensor. The developed sensor provided significant advantages in terms of low detection limit, high stability and good reproducibility for detection of H2O2 in comparison with recently reported electrochemical H2O2 sensors. 相似文献
107.
Application of multiwalled carbon nanotubes for the preconcentration and determination of organochlorine pesticides in water samples by gas chromatography with mass spectrometry 下载免费PDF全文
Abdollah Taghani Naaser Goudarzi Ghadamali Bagherian 《Journal of separation science》2016,39(21):4219-4226
A fast, sensitive, and convenient technique consisting of a miniaturized solid‐phase extraction method named microextraction in packed syringe coupled with gas chromatography and mass spectrometry was developed for the preconcentration and determination of some pesticides, including hexachlorobenzene, heptachlor, alachlor, aldrine, and metolachlore, in natural water samples. Carboxyl‐purified multiwalled carbon nanotubes were used as a sorbent in microextraction in packed syringe. Based on this technique, 6.0 mg of multiwalled carbon nanotubes was inserted in the syringe between two polypropylene frits. The analytes would be adsorbed on the solid phase, and would subsequently be eluted using organic solvents. The influence of some important parameters involved including the solution pH, type, and volume of the organic desorption solvent, and amount of the multiwalled carbon nanotubes sorbent on the extraction efficiency of the selected pesticides were investigated. The proposed method showed a good linearity in the range of 0.1–25.0 ng/mL and low limits of detection in the range of 0.02–0.19 ng/mL using the selected ion‐monitoring mode. Reproducibility of the method was in the range of 3.3–8.5% for the studied pesticides. Also to evaluate the matrix effect, the developed method was applied to the preconcentration and determination of the selected pesticides in different water samples. 相似文献
108.
Titanium was incorporated in ionic liquid based periodic mesoporous organosilica to prepare a nanostructured catalyst (Ti@PMO‐IL) with high activity. Procedure for the synthesis of Ti@PMO‐IL was followed according the simultaneous hydrolysis and condensation of alkylimidazolium ionic liquid, tetramethoxysilane (TMOS) and tetrabutylorthotitanate (TBOT) where a surfactant template was used together with a simple acid‐based catalytic aproach. N2 adsorption isotherm of the Ti@PMO‐IL was studied to measure its mean pore volume, pore size distribution and specific surface area. Diffuse reflectance infrared Fourier transform (DRIFT) spectroscopy was applied to identify the chemical bonds present in Ti@PMO‐IL. The morphology of this nanomaterial was investigated by scanning electron microscopy (SEM). Transmission electron microscopy (TEM) image was used to study mesoporosity and structure order of the catalyst. The catalytic activity of Ti@PMO‐IL was then studied and found to be efficient and reusable to catalyze Hantzsch reaction. 相似文献
109.
A simple procedure has been used for preparation of modified glassy carbon electrode with carbon nanotubes and copper complex. Copper complex [Cu(bpy)2]Br2 was immobilized onto glassy carbon (GC) electrode modified with silicomolybdate, α-SiMo12O404− and single walled carbon nanotubes (SWCNTs). Copper complex and silicomolybdate irreversibly and strongly adsorbed onto GC electrode modified with CNTs. Electrostatic interactions between polyoxometalates (POMs) anions and Cu-complex, cations mentioned as an effective method for fabrication of three-dimensional structures. The modified electrode shows three reversible redox couples for polyoxometalate and one redox couple for Cu-complex at wide range of pH values. The electrochemical behavior, stability and electron transfer kinetics of the adsorbed redox couples were investigated using cyclic voltammetry. Due to electrostatic interaction, copper complex immobilized onto GC/CNTs/α-SiMo12O404− electrode shows more stable voltammetric response compared to GC/CNTs/Cu-complex modified electrode. In comparison to GC/CNTs/Cu-complex the GC/CNTs/α-SiMo12O404− modified electrodes shows excellent electrocatalytic activity toward reduction H2O2 and BrO3− at more reduced overpotential. The catalytic rate constants for catalytic reduction hydrogen peroxide and bromate were 4.5(±0.2) × 103 M−1 s−1 and 3.0(±0.10) × 103 M−1 s−1, respectively. The hydrodynamic amperommetry technique at 0.08 V was used for detection of nanomolar concentration of hydrogen peroxide and bromate. Detection limit, sensitivity and linear concentration range proposed sensor for bromate and hydrogen peroxide detection were 1.1 nM and 6.7 nA nM−1, 10 nM-20 μM, 1 nM, 5.5 nA nM−1 and 10 nM-18 μM, respectively. 相似文献
110.