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61.
Ultrasonic butt welding of aluminum,aluminum alloy and stainless steel plate specimens 总被引:3,自引:0,他引:3
Tsujino J Hidai K Hasegawa A Kanai R Matsuura H Matsushima K Ueoka T 《Ultrasonics》2002,40(1-8):371-374
Welding characteristics of aluminum, aluminum alloy and stainless steel plate specimens of 6.0 mm thickness by a 15 kHz ultrasonic butt welding system were studied. There are no detailed welding condition data of these specimens although the joining of these materials are required due to anticorrosive and high strength characteristics for not only large specimens but small electronic parts especially. These specimens of 6.0 mm thickness were welded end to end using a 15 kHz ultrasonic butt welding equipment with a vibration source using eight bolt-clamped Langevin type PZT transducers and a 50 kW static induction thyristor power amplifier. The stainless steel plate specimens electrolytically polished were joined with welding strength almost equal to the material strength under rather large vibration amplitude of 25 microm (peak-to-zero value), static pressure 70 MPa and welding time of 1.0-3.0 s. The hardness of stainless steel specimen adjacent to a welding surface increased about 20% by ultrasonic vibration. 相似文献
62.
Harano Azuchi Shimada Koji Okubo Tatsuya Sadakata Masayoshi 《Journal of nanoparticle research》2002,4(3):215-219
Titanium dioxide ultrafine particles (UFPs) are produced by pulsed laser ablation of titanium or titanium dioxide (anatase and rutile) rods in an atmosphere of He or O2/He mixture. The collected UFPs on cellulose membrane filters at the exit of the ablation chamber are analyzed by X-ray diffraction (XRD) and transmission electron microscopy (TEM). The TiO2 particles produced are composed of very small particles (diameter: 10–50nm) that are completely anatase, irrespective of the rod material, and relatively large particles (diameter: 100nm–1m) that are a mixture of anatase and rutile. The large particles consist of the direct strip-off fragments coming from the rod surface. The particles obtained from the laser ablation on TiO2 rods in an atmosphere of He contains gray particles that are supposed to be amorphous TiO2 (x < 2). In the presence of O2 in the ablation chamber, these oxygen defects in amorphous TiO2 are stabilized and anatase UFPs are formed. These results suggest that the crystal phase of the products can be controlled by adjusting the rod material and the gases used in the ablation process. 相似文献
63.
64.
S. Nara S. Shimada H. Kashiwabara J. Sohma 《Journal of Polymer Science.Polymer Physics》1968,6(8):1435-1449
Decay reactions of the free radicals produced in irradiated polyethylene (high-density and low-density materials) were examined in connection with the molecular motion of the matrix polymer. Three temperature regions, in which the free radicals decay very rapidly, at around 120, 200, and 250°K, were designated TA, TL, and TB, respectively. The decay of the free radicals at these temperatures had activation energies in high-density polyethylene of 0.4 kcal/mole for TA, 9.4 kcal/mole for TL, and 18.4 kcal/mole for TB. In low-density polyethylene these quantities were 0.7 kcal/mole for TA, 23.1 kcal/mole for TL, and 24.8 kcal/mole for TB. Comparison of time constants for the decay reactions and for molecular motion of the matrix polymer indicate that the decay in TA and TB is closely related to molecular motion in the amorphous regions of the polymer. The decay of the free radicals at TL in high-density polyethylene is due to molecular motion associated with local mode relaxation at lamellar surfaces, while that of low-density polyethylene is due to local mode relaxation in the completely amorphous region. Steric configurations of the free radicals which decay in the respective temperature regions were also investigated. 相似文献
65.
The crystallographic and magnetic properties of the compounds InM2+CrS4(M = Mn, Fe, Co, Ni) were studied. Three of these compounds except MnInCrS4 were antiferromagnetic. The Néel termperature and paramagnetic Curie temperature were determined to be 20 and 82K for InFeCrS4, 36 and 115K for InCoCrS4 and 22 and 26K for InNiCrS4, respectively. 相似文献
66.
Tsukasa Ikeda Ryoichi Kojin Chul-joong Yoon Hiroshi Ikeda Masao Iijima Kenjiro Hattori Fujio Toda 《Journal of inclusion phenomena and macrocyclic chemistry》1984,2(3-4):669-674
Cyclodextrin (CD) has a hydrophobic cavity which acts like a binding site of an actual enzyme. But enzymatic turnover reaction did not occur in CD-catalyzed reactions. -CD was modified by a histamine group to attach a reactive functional group. -CD-histamine accelerates the hydrolysis of p-nitrophenyl acetate. Catalytic rate constant of this reaction is close to an actual enzyme, -chymotrypsin. Enzymatic turnover reaction is realized with this compound at around neutral pH value. 相似文献
67.
Aiura Y Yoshida Y Hase I Ikeda SI Higashiguchi M Cui XY Shimada K Namatame H Taniguchi M Bando H 《Physical review letters》2004,93(11):117005
We present detailed energy dispersions near the Fermi level along the high symmetry line GammaX on the monolayer and bilayer strontium ruthenates Sr2RuO4 and Sr3Ru2O7, determined by high-resolution angle-resolved photoemission spectroscopy. A kink in the dispersion is clearly shown for the both ruthenates. The energy position of the kink and the slope in the low-energy part near the Fermi level are almost identical between them, whereas the dispersion in the high-energy part varies, like the behavior of the kink for the cuprate superconductors. 相似文献
68.
A new coordination mode of hydrotris(2-mercaptoimidazolyl)borate ligands was found in the reaction of [Na(Tm(tBu))] with Me(2)BiCl to form a trinuclear organobismuth complex [(Me(2)Bi)(3)(Tm(tBu))(2)](+)[Me(2)BiCl(2)](-)(Tm(tBu)= hydrotris(2-mercapto-1-tert-butylimidazolyl)borate). 相似文献
69.
70.
Development of a novel analytical method for determination of chondroitin sulfate using an in-capillary enzyme reaction 总被引:3,自引:0,他引:3
A novel analytical method for determination of total amount of chondroitin sulfate (CS) based on its conversion to desulfated chondro-disaccharide via an enzyme-catalyzed reaction, was developed. Using the in-capillary enzyme reaction, the method was also applied to the successful construction of an on-line analytical system. Within this system, electrophoretic migration was used to mix zones containing the enzyme mixture (chondroitinase ABC, chondro-4-sulfatase, chondro-6-sulfatase and 2-o-sulfatase) and the substrate (CS). The reaction was then allowed to proceed in the presence of a weak electric field and, finally, the product (desulfated chondro-disaccharide) of enzyme reaction migrated to the detector under the influence of an applied electric field. A polyvinyl alcohol-coated capillary was used to reduce protein adsorption. Desulfated chondro-disaccharide was successfully migrated toward the anode in 10 mM Tris-acetate buffer (pH 7.0) under reversed polarity and detected at 232 nm. The established method was validated and demonstrated to be applicable in the determination of total amount of CS in a commercial ophthalmic solution. No interference from the formulation excipients was observed. Good linearity was obtained, with correlation coefficients above 0.999. Recoveries and precisions ranged from 100.0 to 100.5%, and from 0.2 to 0.6% of the relative standard deviation, respectively. Good agreement was obtained between the established method and traditional photometric method based on carbazole reaction. In this study, application of the method to disaccharide compositional analysis was also performed. 相似文献