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91.
Experiments have been carried out to determine heat transfer rates from a continuously moving belt to an air jet impinging normally. The parameters that were varied included the jet velocity (4 < VN < 40 m/s), the jet width (4.8 < B < 19 mm), the nozzle-to-plate distance (3 < H/2B < 11) and the belt speed (0. 15 < VB < 5. 5 m/s). An infrared thermometer was used for the measurement of temperature of the moving belt. The average heat transfer coefficients increase with belt speed steeply initially to a maximum value and then remain almost constant for all higher belt speeds. The maximum heat transfer coefficients are about 1.5 to 2.0 times higher than those predicted for the stationary surface. The present data on continuously surface in still air and in impinging jet flow are well compared with the data on rotating cylinders reported in the literature.
Nomenclature A Heat transfer area - B Width of the nozzle - D Diameter of the cylinder or equivalent diameter of the flat surface (D=L/) - k Thermal conductivity - Gr Grashof number - h Heat transfer coefficient - H Height of the nozzle from the surface - i Number of nozzles - L Heat transfer length of a flat surface - NuD Nusselt number hD/k - ReDB Belt Reynoldsnumber, DVB/ - ReDN Nozzle Reynolds number, DVN/ - ReSN Nozzle Reynolds number, SVN/ - S Hydraulic diameter of the nozzle, 2B - VB Belt velocity or circumferential velocity of a cylinder - VN Nozzle celocity - Kinematic viscosity 相似文献
Wärmeübergang zwischen einem senkrecht auftreffenden Strahl und einer bewegten Oberfläche
Zusammenfassung Experimentell bestimmte Wärmeübergangskoeffizienten für Düsengeschwindigkeiten zwischen 4 m/s und 40 m/s, sowie Düsenbreiten zwischen 4,8 mm und 19 mm lagen bei Bandgeschwindigkeiten zwischen 0, 15 m/s bis 5, 5 m/s ca. 50 % bis 100 % höher als bei unbewegtem Band. Die gemessenen Daten bei bewegtem wie bei unbewegtem Band schließen gut an bekannte Werte aus der Literatur an.
Nomenclature A Heat transfer area - B Width of the nozzle - D Diameter of the cylinder or equivalent diameter of the flat surface (D=L/) - k Thermal conductivity - Gr Grashof number - h Heat transfer coefficient - H Height of the nozzle from the surface - i Number of nozzles - L Heat transfer length of a flat surface - NuD Nusselt number hD/k - ReDB Belt Reynoldsnumber, DVB/ - ReDN Nozzle Reynolds number, DVN/ - ReSN Nozzle Reynolds number, SVN/ - S Hydraulic diameter of the nozzle, 2B - VB Belt velocity or circumferential velocity of a cylinder - VN Nozzle celocity - Kinematic viscosity 相似文献
92.
Ahyi AC Cao H Raju PK Uberall H 《The Journal of the Acoustical Society of America》2005,118(1):124-128
We consider evacuated thin semi-infinite shells immersed in a fluid, which may be either of cylindrical shape with a hemispherical shell endcap, or formed two-dimensionally by semi-infinite parallel plates joined together by a semi-cylinder. The connected shell portions are joined in a manner to satisfy continuity but with a discontinuous radius of curvature. Acoustic waves are considered incident along the axis of symmetry (say the z axis) onto the curved portion of the shell, where they, at the critical angle of coincidence, generate Lamb and Stoneley-type waves in the shell. Computations were carried out using a code developed by Cao et al. [Chinese J. Acoust. 14, 317 (1995)] and was used in order to computationally visualize the waves in the fluid that have been re-radiated by the shell waves a the critical angle. The frequency range was below that of the lowest Lamb wave, and only the A0 wave (and partly the S0 wave) was observed to re-radiate into the fluid under our assumptions. The results will be compared to experimental results in which the re-radiated waves are optically visualized by the Schardin-Cranz schlieren method. 相似文献
93.
M. Ramesh B. Raju M. George K. Srinivas V. Jayathirtha Rao K. Bhanuprakash R. Srinivas 《Journal of mass spectrometry : JMS》2012,47(7):860-868
The electrospray ionization collisionally activated dissociation (CAD) mass spectra of protonated 2,4,6‐tris(benzylamino)‐1,3,5‐triazine (1) and 2,4,6‐tris(benzyloxy)‐1,3,5‐triazine (6) show abundant product ion of m/z 181 (C14H13+). The likely structure for C14H13+ is α‐[2‐methylphenyl]benzyl cation, indicating that one of the benzyl groups must migrate to another prior to dissociation of the protonated molecule. The collision energy is high for the ‘N’ analog (1) but low for the ‘O’ analog (6) indicating that the fragmentation processes of 1 requires high energy. The other major fragmentations are [M + H‐toluene]+ and [M + H‐benzene]+ for compounds 1 and 6, respectively. The protonated 2,4,6‐tris(4‐methylbenzylamino)‐1,3,5‐triazine (4) exhibits competitive eliminations of p‐xylene and 3,6‐dimethylenecyclohexa‐1,4‐diene. Moreover, protonated 2,4,6‐tris(1‐phenylethylamino)‐1,3,5‐triazine (5) dissociates via three successive losses of styrene. Density functional theory (DFT) calculations indicate that an ion/neutral complex (INC) between benzyl cation and the rest of the molecule is unstable, but the protonated molecules of 1 and 6 rearrange to an intermediate by the migration of a benzyl group to the ring ‘N’. Subsequent shift of a second benzyl group generates an INC for the protonated molecule of 1 and its product ions can be explained from this intermediate. The shift of a second benzyl group to the ring carbon of the first benzyl group followed by an H‐shift from ring carbon to ‘O’ generates the key intermediate for the formation of the ion of m/z 181 from the protonated molecule of 6. The proposed mechanisms are supported by high resolution mass spectrometry data, deuterium‐labeling and CAD experiments combined with DFT calculations. Copyright © 2012 John Wiley & Sons, Ltd. 相似文献
94.
A. Dhal R. K. Sinha D. Negi T. Trivedi M. K. Raju D. Choudhury G. Mohanto S. Kumar J. Gehlot R. Kumar S. Nath S. S. Ghugre R. P. Singh J. J. Das S. Muralithar N. Madhavan J. B. Gupta A. K. Sinha A. K. Jain I. M. Govil R. K. Bhowmik S. C. Pancholi L. Chaturvedi 《The European Physical Journal A - Hadrons and Nuclei》2012,48(3):1-10
The odd mass nucleus 137Pm has been studied to high spins through the 109Ag(32S, 2p2n)137Pm reaction at an incident beam energy of 150 MeV. The de-exciting ??-rays were detected using an array of 18 Compton suppressed clover detectors. The level scheme of 137Pm has been extended up to $J^\pi = \tfrac{{43}} {2}^ -$ and excitation energy of E x ? 6 MeV with the observation of 42 new gamma transitions. The linear polarization (IPDCO) measurements for the ??-ray transitions have been done for the first time. The spin and parity assignments for most of the reported levels have been made using these results and the coincidence angular anisotropy (RDCO) measurements. The nuclear shape evolution is discussed in the light of Total Routhian Surface (TRS) and Cranked Shell Model (CSM) calculations. 相似文献
95.
96.
Polymers are an integral part of our daily life. Hence, there are constant efforts towards synthesizing novel polymers with unique properties. As the composition and packing of polymer chains influence polymer''s properties, sophisticated control over the molecular and supramolecular structure of the polymer helps tailor its properties as desired. However, such precise control via conventional solution-state synthesis is challenging. Topochemical polymerization (TP), a solvent- and catalyst-free reaction that occurs under the confinement of a crystal lattice, offers profound control over the molecular structure and supramolecular architecture of a polymer and usually results in ordered polymers. In particular, single-crystal-to-single-crystal (SCSC) TP is advantageous as we can correlate the structure and packing of polymer chains with their properties. By designing molecules appended with suitable reactive moieties and utilizing the principles of supramolecular chemistry to align them in a reactive orientation, the synthesis of higher-dimensional polymers and divergent topologies has been achieved via TP. Though there are a few reviews on TP in the literature, an exclusive review showcasing the topochemical synthesis of polymers with advanced structural features is not available. In this perspective, we present selected examples of the topochemical synthesis of organic polymers with sophisticated structures like ladders, tubular polymers, alternating copolymers, polymer blends, and other interesting topologies. We also detail some strategies adopted for obtaining distinct polymers from the same monomer. Finally, we highlight the main challenges and prospects for developing advanced polymers via TP and inspire future directions in this area.This perspective showcases the potential of topochemical polymerization as an effective tool for synthesizing polymers with advanced molecular and supramolecular structures. 相似文献
97.
Ritesh Raju Oleksandr Gromyko Viktor Fedorenko Andriy Luzhetskyy Rolf Müller 《Tetrahedron letters》2012,53(24):3009-3011
A Streptomyces sp. Lv3-13, isolated from the rhizosphere soil of the plant Mespilus germanica, has yielded three new pimprinine derivatives, named pimprinols A–C (1–3) and the unknown (2-aminophenyl)(2-ethyloxazol-5-yl) methanone (4) along with the known compounds 2-ethyl oxazole pimprinine and 2-propyl oxazole pimprinine. The structures of the compounds were elucidated based on spectroscopic methods including UV, HR-ESIMS and 1D, 2D NMR data. Compounds 1–4 were screened for antimicrobial and cytotoxic activities. 相似文献
98.
P. Sarita G. J. Naga Raju A. S. Pradeep Tapash R. Rautray B. Seetharami Reddy S. Bhuloka Reddy V. Vijayan 《Journal of Radioanalytical and Nuclear Chemistry》2012,294(3):355-361
Trace elemental imbalance in human beings is postulated to exert action, directly or indirectly, on the carcinogenic process. The objective of this study was to evaluate the levels of trace elements in blood sera of breast cancer patients and analyze their alteration with respect to healthy controls. This work was also intended to establish the role played by the trace elements in carcinogenic process. Particle induced X-ray emission (PIXE) technique was used for trace elemental analysis of blood sera of breast cancer patients and healthy controls. The PIXE measurements were carried out using a 2.5?MeV collimated proton beam from the 3 MV Tandem Pelletron accelerator at Institute of Physics, Bhubaneswar, India. On comparing the trace elemental content in the sera of breast cancer patients with those of control subjects, significant variations were observed in the levels of most of the trace elements. The serum levels of almost all the elements except Fe and Cu were observed to be depressed in cancer patients with respect to normal subjects. However, this variation was significant only for Ti (P?<?0.00005), Cr (P?<?0.005), Mn (P?<?0.0005), Ni (P?<?0.01), Zn (P?<?0.000001), and Se (P?<?0.05). On the other hand, significant elevations were observed in serum Fe (P?<?0.05) and Cu (P?<?0.005) levels in cancer patients. The findings presented in this paper give guidelines for future study into the possible roles and interactions of essential trace elements in the breast carcinogenic process. 相似文献
99.
S. Abdul Sattar B. Seetharami Reddy V. Koteswara Rao A. S. Pradeep G. J. Naga Raju K. Ramanarayana P. V. Madhusudana Rao S. Bhuloka Reddy 《Journal of Radioanalytical and Nuclear Chemistry》2012,294(3):337-341
Trace elemental analysis was carried out in various parts of 10 anti-epileptic medicinal plants using PIXE technique. A 3?MeV proton beam was used to excite the samples and spectra were recorded using a Si(Li) detector. Data analysis was done using Gupix Software. The elements Cl, K, Ca, Ti, Mn, Fe, Ni, Cu, Zn, Br and Sr were identified and their concentrations estimated. The presence of some of these trace elements is correlated with the anti-epileptic curative property of these plants. 相似文献
100.
Rama Raju Baadhe Naveen Kumar Mekala Satwik Reddy Palagiri Sreenivasa Rao Parcha 《Applied biochemistry and biotechnology》2012,167(5):1172-1182
In this case study, we designed a farnesyl pyrophosphate (FPP) biosynthetic network using hybrid functional Petri net with extension (HFPNe) which is derived from traditional Petri net theory and allows easy modeling with graphical approach of various types of entities in the networks together. Our main objective is to improve the production of FPP in yeast, which is further converted to amorphadiene (AD), a precursor of artemisinin (antimalarial drug). Natively, mevalonate (MEV) pathway is present in yeast. Methyl erythritol phosphate pathways (MEP) are present only in higher plant plastids and eubacteria, but not present in yeast. IPP and DAMP are common isomeric intermediate in these two pathways, which immediately yields FPP. By integrating these two pathways in yeast, we augmented the FPP synthesis approximately two folds higher (431.16 U/pt) than in MEV pathway alone (259.91 U/pt) by using HFPNe technique. Further enhanced FPP levels converted to AD by amorphadiene synthase gene yielding 436.5 U/pt of AD which approximately two folds higher compared to the AD (258.5 U/pt) synthesized by MEV pathway exclusively. Simulation and validation processes performed using these models are reliable with identified biological information and data. 相似文献