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1.
The large deviation theorems, exponential inequalities and a non-uniform estimate of the Berry–Esséen theorem in a discounted version are proved.Dedicated to Professor Vytautas Statulevičius on the occasion of his 75th birthday. 相似文献
2.
J. Požela A. Namajūnas A. Tamaševičius J. Ulbikas 《Applied Physics A: Materials Science & Processing》1989,48(2):181-188
A method for quantitative characterization of chaotic dynamical systems is discussed. An electronic instrument for determining the number of independent variablesk
*, involved in the motion, is described. It allows one to obtain these in real time from a single observable. The suggested technique has been applied to quantification of strange attractors underlying chaotic instabilities in semi-insulating GaAsCr, and n-Ge, irradiated with high energy electrons. In n-Ge, for instance, the measured numbersk
* range from 2 to 4 depending on control parameters. These measurements reveal the highly deterministic nature of the observed chaotic oscillations. The physical mechanisms responsible for the current instabilities and chaotic behaviour are discussed. 相似文献
3.
The mean-square molecular dipole moments 〈μ2〉 of carbazole, N-ethylcarbazole and of the sequence of poly(epoxypropylcarbazole) (PEPCa) oligomers of various molecular weights have been evaluated in solutions of these organic compounds in dioxan. For PEPCa the values of 〈μ2〉 have also been determined in the solid state. On the basis of the experimental results and of molecular mechanics calculations it has been shown that the orientation of the lateral group of PEPCa favors noninteracting racemic dyads. The temperature-dependence of the effective dipole moment of solid PEPCa follows the Onsager theory above 295 K. 相似文献
4.
Žydrė Šaltienė Natalija Jatulienė Mudis Šalkauskas Daiva Brukštienė Asta Ruzgytė Aušra Tarasevičiūtė Julius Kalibatas 《Accreditation and quality assurance》2005,10(8):444-451
The estimation scheme of uncertainty of determination of 1-hydroxypyrene (1-OHP) in urine was developed analysing the main
stages of the analytical procedure: (1) preparation of 1-OHP standards, (2) creation of the calibration curve for the high
performance liquid chromatography (HPLC) analysis method with the evaluation of recovery, (3) measuring procedure of aliquot
of urine, (4) adjusting the pH of aliquot and hydrolysis with enzyme, (5) solid phase extraction, (6) concentration of the
extract, (7) injection of the extract to chromatograph and analysing by the HPLC method, (8) calculation of 1-OHP mass from
the calibration curve, (9) calculation of 1-OHP concentration in urine. The evaluation of the uncertainty is based on quantification
of individual components. Combined uncertainty was calculated using the law of propagation of uncertainties according to the
EURACHEM/CITAC guidelines. Level dependence of the uncertainty arises from the calibration curve.
The limits of detection and quantification were found to be equal to 0.03 and 0.1 ng/mL, respectively. The calculated expanded
level-dependent uncertainty covers 47–27–25% within the concentration range 0.03–0.1–0.4 ng/mL with the materials and equipment
used. These parameters could easily be recalculated according to the proposed scheme if there are some changes in the analysis
procedure. 相似文献
5.
Electrodes containing glucose oxidase or xanthine oxidase adsorbed on modified glassy carbon electrodes or on conductive complexes, accumulate charge in the presence of substrates, the discharge of which gives the chronoamperometric stripping current. This current is 15 times higher than the stationary current after preconcentration for 8 min. A ten-fold increase in sensitivity of the determination of glucose or hypoxanthine is observed. The stripping current of electrodes based on cytochrome b2 adsorbed on a graphite electrode is 25 times higher than the stationary current. The electrode is useful for lactate determinations for more than 7 days. 相似文献
6.
Ruslan Bikmurzin Rimant Bandzevi
it Arnas Maralka Andrius Maneikis Lilija Kaldien 《Molecules (Basel, Switzerland)》2022,27(14)
β-glucans are known as biological response modifiers. However, different sources can result in structural differences and as a result differences in their biological activity. The hot water extraction method allows to obtain, high molecular weight β-glucans without altering their structure by using strong chemicals, such as alkalis or acids. Analysis of β-glucans by FT-IR and NMR spectroscopy in solid state is superior to analysis in solution as it allows researchers to study the preserved structure of the extracted polysaccharides. FT-IR spectroscopy was used in this study to make side-by-side comparison analysis of hot water extracted β-glucans from different yeast sources. NMR spectroscopy was used to confirm findings made by FT-IR spectroscopy. Extracted β-glucans exhibit characteristic structure of β-1,3/1,6-linked glucans with noticeable levels of proteins, possibly in a form of oligopeptides, chitin and other impurities. β-glucans obtained from C. guilliermondii, P. pastoris and S. pastorianus exhibited higher protein content. Differences in mannan, chitin and α-glucan content were also observed; however, the species-specific structure of obtained β-glucans could not be confirmed without additional studies. Structural analysis of high molecular weight β-glucans in solid state by FT-IR spectroscopy is difficult or limited due to band intensity changes and overlapping originating from different molecules. 相似文献
7.
Thin MoO2 films were electrodeposited on a selenium pre-deposited SnO2|glass plate. The photoelectrochemical properties of MoO2 films were investigated in 0.1 M Na2SO4 solution by the ultraviolet–visible spectrophotometry, linear sweep voltammetry, and altering current impedance measurement techniques. It was found that under illumination with the incident light of λ?=?366 nm, the photo response of the MoO2|SnO2|glass electrode resulted from the MoO2 layer, while the SnO2 layer served as a sink for photogenerated charge carriers. The MoO2 film exhibited n-type conductivity. A schematic band structure diagram of MoO2 in 0.1 M Na2SO4 solution was constructed. The flat band potential (E fb), the donor concentration (N D), the photogeneration current efficiency depended on MoO2 film thickness. The [Fe(CN)6]4?/3? redox PEC cell with MoO2|SnO2|glass plate as a photoanode was constructed. Power output characteristics such as the open circuit voltage (V OC), short circuit current (I SC), the fill factor (FF), and the light-to-electrical conversion efficiency (η) were determined. The maximum light-to-electrical conversion efficiency exhibited by the PEC cell was 0.94 %. 相似文献
8.
G. Lujanienė P. Beneš K. Štamberg K. Jokšas I. Kulakauskaitė 《Journal of Radioanalytical and Nuclear Chemistry》2013,295(3):1957-1967
Sorption of Am and Pu isotopes to bottom sediments of the Baltic Sea has been studied under natural and laboratory conditions. Data obtained from sequential extraction, sorption of Am(III), Pu(IV) and Pu(V) as well as oxidation state distribution experiments have shown that Pu(V) sorption mechanism includes a very fast Pu(V) reduction (reaction rate ≤ 2.33 × 10?3 s?1) to Pu(IV) by humic substances and/or by Fe(II) to Pu(IV) and partly to Pu(III). Following reduction Pu isotopes were bound to various components of bottom sediments via ion exchange and surface complexation reactions and a slow incorporation into the crystalline structure of Fe minerals. Kinetics experiments showed that the sorption of Pu(V), Pu(IV) and Am(III) to bottom sediments from natural seawater was controlled by the inert layer diffusion process. 相似文献
9.
Andrius Garbaras Justina Šapolaitė Inga Garbarienė Žilvinas Ežerinskis Agnė Mašalaitė-Nalivaikė Raminta Skipitytė 《Isotopes in environmental and health studies》2018,54(5):463-474
In the present study, a combination of the stable carbon isotope ratio (13C/12C) with radiocarbon data (14C) allowed us to perform the aerosol source apportionment. Filter samples of PM1 were collected during the warm and cold periods in rural and urban sites in Lithuania. The 14C/12C ratio of total carbon (TC) was measured using the single stage accelerator mass spectrometer quantifying of fossil and non-fossil derived aerosol emissions. The δ13C value was measured using an elemental analyser interfaced with an isotope ratio mass spectrometer. We have found that the highest fraction of contemporary carbon (fc?=?0.82) was measured during a warm period in a rural location. A higher fraction of fossil fuel-derived carbon was observed for air masses transported from highly industrialized Western European regions during both seasons. Isotope mass balance calculations revealed that the traffic emissions composed 15 and 25?% in rural and urban sites, respectively, and did not change during either season. Input from coal-derived aerosol particles was estimated to be 15?% at an urban site during the cold period. The combination of the stable carbon isotope ratio with the radiocarbon data allowed us to distinguish coal, liquid fossil fuel combustion, and non-fossil derived aerosol particle emissions. 相似文献
10.
Monte Carlo study of impact ionization in n-type InAs induced by intense ultrashort terahertz pulses
Electron impact ionization induced in n-type InAs by single-cycle pulses of picosecond and subpicosecond duration has been investigated by Monte Carlo method. It is established that the rate of generation of electron–hole pairs decreases with the decrease of the pulse duration. The impact ionization threshold field is found to depend linearly on frequency for the fields oscillating at frequencies much higher than reciprocal momentum relaxation time. Good agreement between calculations and available experimental data has been obtained. 相似文献