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81.
Prof. N. Riahi 《Acta Mechanica》1986,64(3-4):155-163
Summary Finite amplitude fluid motion is investigated in a horizontal layer of an infinite Prandtl number fluid with an upper free surface for the case where thermocapillary effects are significant and gravitational effects are negligible. It is found that subcritical instability exists and that two-dimensional rolls and down-hexagons (where motion is downward at the cells' centers) are always unstable. But up-hexagons (where motion is upward at the cells' centers) are stable for sufficiently small amplitude , while both uphexagons and squares are stable in a range of larger where hysteresis effects exist.With 1 Figure 相似文献
82.
Prof. Dr. A. Kaveh 《Acta Mechanica》1986,62(1-4):189-196
Summary A combinatorial method is presented for examining the rigidity of planar structures. In this approach, an expansion process is used for the formation of a statically determinate substructure, known as a -tree of a structure. The algorithm of Lováz and Yemini, and the method of Sugihara are employed for the recognition of the elementary subgraphs, during this process.With 4 Figures 相似文献
83.
Summary The family of f.c.c. crystal orientations defined by loading direction (110) and any channel die constraint direction between (
) and (
) is kinematically unstable. We establish that the experimentally observed finite rotation of the lattice about the loading axis, for initial orientations in this range, is uniquely predicted by the constraints and critical slip-system inequalities without regard to particular hardening theory. We further establish that experimental information on the changing constraint stress would serve to distinguish among theories. Predictions of three specific hardening rules, including classical Taylor hardening and the simple theory, are illustrated for initial constraint directions (
) and (
). For the first of these orientations the predictions include constraint stress, lattice rotation, active and latent hardening, and overall crystal shearing to a logarithmic compressive strain of 1.0. 相似文献
84.
Summary Three real gas isentropic exponentsk
Tv,k
rv,k
pT are introduced, which when used in place of the classical isentropic exponentk=c
p/c in the ideal gas isentropic change equations, the latter may describe very accurately the isentropic change of real gases. The usual practice of employing exponentk may lead to considerably incorrect results even when the value ofk corresponds to the correct local value ofc
p/c
v of the real gas under examination. The numerical values of the new exponents are calculated in the case of real air for temperatures from 150 K to 450 K and pressures from 1 bar to 1000 bar. It is seen that at low temperatures and high pressures the values of the new exponents differ considerably from the values of the classical exponentk. Therefore, the error resulting by approximating, as is usually the case, the behaviour of real gases by the ideal gas isentropic change equations in a stepwise fashion with exponentk instead of the new exponents, is considerable. It follows that exponentk, which appears in various relations in thermodynamics, fluid mechanics, gasdynamics, heat transfer etc., should be suitably replaced by combinations of the three exponents. Related numerical examples, made in the case of real air, showed that the use ofk leads (in the temperature and pressure ranges examined) to a 5% error in the calculation of blowby rate in internal combustion enginers, high pressure compressors or steam turbines and to a 50% error in the calculation of the isentropic expansion or compression.Nomenclature
A
ij,B
i,N
ij,O
ij,Q
ij
Coefficients
-
c
Velocity
-
c
p
Specific heat under constant pressure
-
c
v
Specific heat under constant volume
-
h
Specific enthalpy
-
k
Isentropic exponent,k=c
p/c
v
-
k
pT
Real gas isentropic exponent corresponding to the pair of variablesp,T
-
k
pv
Real gas isentropic exponent corresponding to the pair of variablesp, v
-
k
Tv
Real gas isentropic exponent corresponding to the pair of variablesT,v
-
M
Mach number,M=c/
-
p
Pressure
-
p
c
Pressure at the critical point
-
R
Constant of the air,R=287.22 J/kg K
-
s
Specific entropy
-
T
Temperature
-
T
c
Temperature at the critical point
-
v
Specific volume
-
v
c
Specific volume at the critical point
-
z
Compressibility factor
-
Sound velocity
- T
Temperature increment
With 14 Figures 相似文献
85.
Prof. D. Karamanlidis 《Acta Mechanica》1987,68(1-2):57-69
Summary The paper deals with the systematic development of variational methods and associated finite element schemes for the approximate analysis of elastoplastic continua. The major difference between these novel models and existing ones consists in treating the yield condition as an a posteriori (natural) constraint and not as an a priori (essential) constraint. The advantages of this approach over existing ones are pointed out and discussed from a theoretical and a computational standpoint as well.With 1 Figure 相似文献
86.
Wei Ren Fuchun Nan Dr. Shumu Li Prof. Sijin Yang Prof. Jiechao Ge Prof. Zhenwen Zhao 《ChemMedChem》2021,16(4):646-653
Negatively charged fluorescent carbon dots (CDs, Em=608 nm) were hydrothermally prepared from thiophene phenylpropionic acid polymers and then successfully loaded with the positively charged anticancer cargo coptisine, which suffers from poor bioavailability. The formed CD-coptisine complexes were thoroughly characterized by particle size, morphology, drug loading efficiency, drug release, cellular uptake and cellular toxicity in vitro and antitumor activities in vivo. In this nano-carrier system, red emissive CDs possess multiple advantages as follows: 1) high drug loading efficiency (>96 %); 2) sustained drug release; 3) enhanced drug efficacy towards cancer cells; 4) EPR effect; 5) drug release tracing with near-infrared imaging. These properties indicated that red emissive CDs prepared from polymers could be used as a novel drug delivery system with integrated therapeutic and imaging functions in cancer therapy, which are expected to have great potential in future clinical applications. 相似文献
87.
Dr. Armin Welker Dr. Christian Kersten Dr. Christin Müller Dr. Ramakanth Madhugiri Collin Zimmer Patrick Müller Robert Zimmermann Stefan Hammerschmidt Hannah Maus Prof. John Ziebuhr Prof. Christoph Sotriffer Prof. Tanja Schirmeister 《ChemMedChem》2021,16(2):340-354
Inhibition of coronavirus (CoV)-encoded papain-like cysteine proteases (PLpro) represents an attractive strategy to treat infections by these important human pathogens. Herein we report on structure-activity relationships (SAR) of the noncovalent active-site directed inhibitor (R)-5-amino-2-methyl-N-(1-(naphthalen-1-yl)ethyl) benzamide ( 2 b ), which is known to bind into the S3 and S4 pockets of the SARS-CoV PLpro. Moreover, we report the discovery of isoindolines as a new class of potent PLpro inhibitors. The studies also provide a deeper understanding of the binding modes of this inhibitor class. Importantly, the inhibitors were also confirmed to inhibit SARS-CoV-2 replication in cell culture suggesting that, due to the high structural similarities of the target proteases, inhibitors identified against SARS-CoV PLpro are valuable starting points for the development of new pan-coronaviral inhibitors. 相似文献
88.
Prof. Alessia Carocci Dr. Mariagrazia Roselli Prof. Roberta Budriesi Dr. Matteo Micucci Prof. Jean-François Desaphy Dr. Concetta Altamura Dr. Maria Maddalena Cavalluzzi Dr. Maddalena Toma Dr. Giovanna Ilaria Passeri Dr. Gualtiero Milani Dr. Angelo Lovece Prof. Alessia Catalano Dr. Claudio Bruno Dr. Annalisa De Palma Prof. Filomena Corbo Prof. Carlo Franchini Prof. Solomon Habtemariam Prof. Giovanni Lentini 《ChemMedChem》2021,16(3):578-588
Under the hypothesis that cardioprotective agents might benefit from synergism between antiarrhythmic activity and antioxidant properties, a small series of mexiletine analogues were coupled with the 2,2,5,5-tetramethylpyrroline moiety, known for its antioxidant effect, in order to obtain dual-acting drugs potentially useful in the protection of the heart against post-ischemic reperfusion injury. The pyrroline derivatives reported herein were found to be more potent as antiarrhythmic agents than mexiletine and displayed antioxidant activity. The most interesting tetramethylpyrroline congener, a tert-butyl-substituted analogue, was at least 100 times more active as an antiarrhythmic than mexiletine. 相似文献
89.
Dr. Bo Zhou Zhengxi Guo Zhaoxin Lin Prof. Bang-Ping Jiang Prof. Xing-Can Shen 《ChemMedChem》2021,16(6):919-931
Phototherapy, a type of photoresponsive regulation of biological activities, together with additional stimuli-responsive features, offers significant potential for enhancing the precision and efficacy of cancer treatments. To achieve tumor-specific therapeutics, numerous studies have focused on the development of smart phototherapeutic nanomaterials (PNMs) that can respond to endogenous pathological characteristics (e. g., mild acidity, the overproduction of glutathione, the overproduction of hydrogen peroxide, the overexpression of specific surface receptors, etc.) present in the tumor and/or exogenous stimuli. Such responsiveness can effectively improve the physicochemical properties, cellular uptake, tumor-targeting performance, and pharmacokinetic profile of PNMs. Herein, we will systematically discuss recent advances in this field. Moreover, potential challenges and future directions in the development of stimuli-responsive PNMs are also presented to support the development of this emerging cutting-edge research area. 相似文献
90.
Dr. Zhichao Du Dr. Guolong Li Dr. Haixia Ge Xiaoyang Zhou Prof. Jian Zhang 《ChemMedChem》2021,16(9):1488-1498
To systematically evaluate the impact of neoglycosylation upon the anticancer activities and selectivity of steroids, four series of neoglycosides of diosgenin, pregnenolone, dehydroepiandrosterone and estrone were designed and synthesized according to the neoglycosylation approach. The structures of all the products were elucidated by NMR analysis, and the stereochemistry of C20-MeON-pregnenolone was confirmed by crystal X-ray diffraction. The compounds′ cytotoxicity on five human cancer cell lines was evaluated using a Cell Counting Kit-8 assay, and structure–activity relationships (SAR) are discussed. 2-deoxy-d -glucoside 5 k displayed the most potent antiproliferative activities against HepG2 cells with an IC50 value of 1.5 μM. Further pharmacological experiments on compound 5 k on HepG2 cells revealed that it could cause morphological changes and cell-cycle arrest at the G0/G1 phase and then induced the apoptosis, which might be associated with the enhanced expression of high-mobility group Box 1 (HMGB1). Taken together, these findings prove that the neoglycosylation of steroids could be a promising strategy for the discovery of potential antiproliferative agents. 相似文献