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1.
The influence of an aggressive environment (0.6 M, aerated NaCl solution) on short fatigue crack initiation and growth behaviour has been studied. The study involved three major test series, namely: air fatigue, corrosion fatigue, and intermittent air fatigue/corrosion fatigue. The above tests carried out under fully reversed torsional loading conditions at a frequency of 5 Hz, showed that it was the non-metallic inclusions which took part in crack initiation resulting from debonding at metal matrix/inclusion interface and pitting of inclusions in both air and corrosove environments, respectively. Short fatigue crack growth results in these two environments obtained by using plastic replication technique, indicated a large effect of microstructure i.e. prior austenite grain boundaries. The stage/stages at which the environmental contribution was dominant has been discussed by considering the results achieved from intermittent tests. However, the mechanisms involved in corrosion fatigue short crack growth have also been described in the light of results obtained from futher investigations carried out by conducting corrosion fatigue tests under applied cathodic potential conditions and tests on hydrogen pre-charged specimens under air fatigue and uniaxial tension conditions. 相似文献
2.
Mamata Mukhopadhyay Sameer V Dalvi 《Journal of chemical technology and biotechnology (Oxford, Oxfordshire : 1986)》2005,80(4):445-454
A supercritical antisolvent (SAS) process is employed for production of solid nanoparticles from atomized droplets of dilute solution in a flowing supercritical carbon dioxide (SC CO2) stream by attaining extremely high, very rapid, and uniform supersaturation. This is facilitated by a two‐way mass transfer of CO2 and solvent, to and from the droplet respectively, rendering rapid reduction in equilibrium solubility of the solid solute in the ternary solution. The present work analyses the degree of supersaturation and nucleation kinetics in a single droplet of cholesterol solution in acetone during its flight in a flowing SC CO2 stream. Both temperature and composition are assumed to be uniform within the droplet, and their variations with time are calculated by balancing the heat and mass transfer fluxes to and from the droplet. The equilibrium solubility of cholesterol with CO2 dissolution has been predicted as being directly proportional to the Partial Molar Volume Fraction (PMVF) of acetone in the binary (CO2–acetone) system. The degree of supersaturation has been simulated up to the time required to attain almost zero cholesterol solubility in the droplet for evaluating the rate of nucleation and the size of the stable critical nuclei formed. The effects of process parameters have been analysed in the pressure range of 7.1–35.0 MPa, temperature range of 313–333 K, SC CO2 flow rate of 0.1136–1.136 mol s?1, the ratio of the volumetric flow rates of CO2‐to‐solution in the range of 100–1000, and the initial mole fraction of cholesterol in acetone solution in the range of 0.0025–0.010. The results confirm an extremely high and rapid increase in degree of supersaturation, very high nucleation rates and stable critical nucleus diameter of the order of a nanometre. Copyright © 2005 Society of Chemical Industry 相似文献
3.
The phenomena of natural convection caused by a concentration gradient usually creates currents as a result of buoyancy forces. These forces are formed from the combined effect of a fluid density gradient and the body force (gravitational force). The above phenomenon was studied experimentally in a circular glass column of 0.08 m diameter and 1 m length. This column was erected vertically and filled with distilled water with a salt bag placed on top of it and partially immersed in water. The dissolution mechanism was then modelled and a finite difference method was used to solve the formulated equations by using the implicit scheme of MacCormack (Anderson et al., 1984). The experimental results and the numerical predictions are represented graphically and give compatible agreement. 相似文献
4.
Phase-separated domains prepared in the two-phase region were dissolved at a temperature in the single-phase region, and their dissolution dynamics was studied by using the time-resolved light scattering (TRLS) technique and a scanning electron microscope (SEM). The time tps of preparation of domains was chosen to be long enough for phase separation to proceed into the late stage. The scattered light intensity at small wavenumbers increased before it attenuated. As tps increased, the increase at smaller wavenumbers became more significant and the peak intensity decreased only slightly with dissolution time. The characteristic wavenumber qm evaluated from TRLS and SEM followed the power-law relation qmt−0.3. 相似文献
5.
阐述了一个全新的聚丙烯腈高聚物溶解理论,取代了以往人们思维中的高聚物大分子必须经过先溶胀再溶解的漫长的静态溶解过程。对于年产50kt/a腈纶装置可减少一次性投资约1500万元,减少运转费用360万元/a,在现有腈纶大装置上实施,经济效益十分可观。 相似文献
6.
初至波走时层析成像中的正则化方法 总被引:2,自引:0,他引:2
波场的等效性、观测数据的有限性和观测误差等因素导致地球物理反演本身具有严重的多解性,降低这种多解性的一种重要途径就是对反演过程进行约束。传统的初至波走时层析成像方法,通常是在外部对模型空间施加显式的约束和平滑处理,这样就会破坏模型参数与传播算子之间的相关性,难以达到有效利用先验信息的目的, 甚至会影响反演的稳定性。针对这一问题,本文将先验信息分为三类,在此基础上阐述了通过正则化手段将各种先验信息纳入到反演方程当中,替代传统的外部约束模式。理论试验结果表明,正则化方法比外部约束方法有效地提高了反演的精度和分辨率;将该正则化方法应用于实际二维资料处理,也得到了比较好的反演结果。 相似文献
7.
La在KCl-NaCl和LaCl_3-KCl-NaCl熔体中的溶解行为SCIEI 总被引:1,自引:0,他引:1
本文利用透明槽技术、电化学循环V-A法及量子化学EHMO三种方法,研究了La在KCl-NaCl(1:1mol)及LaCl_3-KCl-NaCl熔体中的溶解行为。初步认为:溶解在KCl-NaCl熔体中的La是以中性金属状态存在。在LaCl_3-KCl-NaCl熔体中,溶解的La与La^(3+)作用生成低价La^(2+)离子,La^(2+)又与周围的La^(3+)作用形成原子簇离子La_m^(n+)赋存于熔体之中。 相似文献
8.
B. Stypuła J. Banaś M. Starowicz H. Krawiec A. Bernasik A. Janas 《Journal of Applied Electrochemistry》2006,36(12):1407-1414
The anodic behaviour of copper was investigated in ethanol solution containing LiClO4, LiCl electrolyte and water. The type of electrolyte and the water content influences the mechanism of the anodic process and the formation of anodic products. In LiClO4 electrolyte the dissolution of copper is related to the oxidation of Cu(I) to Cu(II). In solutions of LiCl the etching of copper begins with the creation of soluble complexes of Cu(I) with chloride ions and solvent molecules. At potentials above 0.4 V the formation of alkoxides was observed in both solutions, characterized by a yellow tint. On the other hand, above 0.8 V (i.e. above the equilibrium potential of alcohol oxidation) copper dissolution is accompanied by the formation of a blue colloidal suspension of Cu (II) copper salt. Anodic etching of copper in solutions containing 3% H2O at potentials higher than 0.4 V leads to the formation of colloidal suspension of copper oxide nanoparticles. 相似文献
9.
The electrochemical behaviour of the chromium electrode in borate buffer solution (pH 9.3) was studied by cyclic voltammetry and electrochemical impedance spectroscopy. Chromium passivity was observed over a broad potential region, from –1.0 to 0.5 V vs SCE. The passivation process took place in two steps: formation of a chromium oxide monolayer and transition of chromium to a higher valence state. The anodic film exhibited the properties of a p-type semiconductor. Transpassive dissolution of chromium occurred at 0.5 V vs SCE, with two reaction intermediates present, CrCr
III and Crad
4+. 相似文献
10.